CAREFUSION 2200, INC.

FDA Device Registration & Listing · Mannford, OK, US · Registration 1625685

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1625685
FEI Number
1625685
Entity Name
CAREFUSION 2200, INC.
City/State/Country
Mannford, OK, US
Establishment Address
400 East Foster Rd, Mannford, OK 74044, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
CAREFUSION (Owner Number: 10030506)
Owner / Operator Contact Address
75 N Fairway Dr, Vernon Hills, IL 60061, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Safe-T™ PLUS Safe-T-Centesis™ Thora-Para BD Trek™ Bone Marrow Biopsy System BD Trek™ Bone Lesion Biopsy System BD Trek™ Power Driver BD Trek™ Sterile Sleeve T-Handle Jamshidi Bone Marrow Biopsy/Aspiration Needle Jamshidi Evolve Bone Marrow Biopsy/Aspiration Needle Jamshidi Bone Marrow Biopsy/Aspiration Needle T-Handle Jamshidi Bone Marrow Biopsy and Aspiration Trays Safe-T PLUS Trays Jamshidi Evolve Bone Marrow Biopsy and Aspiration Trays Safe-T PLUS Tray Illinois Bone Marrow Aspiration Tray Illinois Bone Marrow Aspiration Needle T-Handle Illinois Bone Marrow Aspiration Needle T-Handle Illinois Bone Marrow Aspiration Tray 42-4016, Introducer Kit BD Curve Ascites Shunt 42-4012, Introducer Kit

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PNG Peritoneal, Drainage Catheter For Refractory Ascites, Long-Term Indwelling Gastroenterology, Urology Class 2 876.5630 2016-11-22
PXI Thoracentesis Tray General Hospital Class 2 880.5570 2019-04-15
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2022-03-30
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2017-09-12
LWE Bone Marrow Collection/Transfusion Kit Unknown Class 2 N/A 2009-10-12
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2009-10-12
KPM Shunt, Peritoneal Gastroenterology, Urology Class 2 876.5955 2009-10-12
KPM Shunt, Peritoneal Gastroenterology, Urology Class 2 876.5955 2018-02-07
DYB Introducer, Catheter Cardiovascular Class 2 870.1340 2018-02-07

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CAREFUSION
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
9680904 CareFusion D.R. 203 Ltd. SANTO DOMINGO Distrito Nacional, DO
1423507 CAREFUSION 2200, INC. Vernon Hills, IL, US
3004932373 CareFusion 213 LLC EL PASO, TX, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K172344 Medax Srl Unipersonale Medax Biopsy Systems II (MEDONE, MEDCUT, MEDEM, MEDBONE, MEDLOCK) 2017-11-13
K812404 Nu Tech Medical Systems BUTTERFLY NEEDLE ASSEMBLY 1981-09-09
K101883 St Jude Medical 6F ENGAGE/ENGAGE TR INTRODUCER 2010-09-07
K034025 Nmt Medical, Inc. NMT MEDICAL TRANSSEPTAL SHEATH SET, MODELS TSS-10-HSC, TSS-11-HSC, TSS12-HSC 2004-03-26
K122854 Arrow International (Subsidiary of Teleflex Inc.) ARROW GLIDETHRU PEEL-AWAY SHEATH/DILATOR INTRODUCER 2013-01-04

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0027-2024 Bard Peripheral Vascular Inc 2
Bard Marquee Disposable Core Biopsy Instrument Kit, REF: MQK2016
Z-0028-2013 Remington Medical Inc. 2
Automatic Cutting Needles, Soft Tissue Biopsy Needle, NAC-1820M, Sterile, Remington Medical, Inc., 5830 Meadowridge Court, Alpharetta, GA 30005. Prostate Biopsy Needles shall be single use only and are to be used by a Urologist in a healthcare setting to obtain needle biopsies of the prostate. The needles are compatible with the Bard Magnum biopsy instrument. The needles have an echogenic tip for accurate placement under ultrasound guidance and centimeter markings along the cannula to facilitate depth placement.
Z-0042-2014 Atossa Genetics, Inc. 2
Brand: The ForeCYTE Breast Health Test, Mammary Aspiration Specimen Cytology Test (MASCT), MASCT System Kits, Clarity System Kits, MASCT Patient Sample Kits & Clarity Patient Sample Kits Instrument, Biopsy. The MASCT System Kit, Patient Sample Kits, or the Nipple Aspirate Fluid Laboratory Kit has the following codes: PRODUCT CODE: AG-MASCT; AG-FC5; DTG-MASCT, DTG-FC5, and NRLBH-5. PART NUMBER: 9002513; 9002513MD; 9002528; 9002528MD; 9002587; 9002614; and 9002717MD. THE MASCT SYSTEM KIT CONSISTS OF: 1. MASCT Breast Pump; 2. Instructions for Use (IFU); 3. Heating Pad; 4. Timer; 5. Saccomono's Fixative; 6. Nu Prep Gel; 7. Welcome and Training Materials Coversheet; 8. MASCT System Order Form; 9. ForeCYTE Training Video DVD; 10. MASCT System Instructions with pictures - pink; THE PATIENT SAMPLE KIT CONSISTS OF: 1. Two (2) flower assemblies (e.g., filter, filter retainer, and filter holder); 2. Instructions for Use (IFU); 3. Two (2) specimen collection devices; 4. Two (2) breast bags for transporting the specimen collection container; 5. Barcode labels; 6. Saccomono's Fixative; 7. Nu Prep Gel; 8. MASCT System package insert; 9. ForeCYTE Test Requisition Form; 10. Patient Information Sheet; 11. Atossa Patient Information; 12. FED EX Clinical PAK; 13. MASCT System Order Form; 14. FED EX Pouch; 15. FED EX Airbill; Product Usage: The MASCT Device is intended for use in the collection of nipple aspirate fluid for cytological testing. The collected fluid can be used in the determination and/or differentiation of normal versus premalignant versus malignant cells.
Z-0044-2018 Bard Peripheral Vascular Inc 2
BARD MAX-CORE Disposable Core Biopsy Instrument, Product Codes - MC1410, 14 g x 10 cm; MC1616, 16 g x 16 cm; MC1816, 18 g x 16 cm; MC1820, 18 g x 20 cm; MC1825, 18 g x 25 cm. The core needle biopsy device is intended for use in obtaining biopsies from soft tissues.
Z-0002-2022 Bard Peripheral Vascular Inc 2
REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1625685. Last updated year: 2026. Please use registration number 1625685 when referencing this establishment in official correspondence.
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