NORFOLK MEDICAL PRODUCTS, INC.

FDA Device Registration & Listing · Skokie, IL, US · Registration 1450392

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
1450392
FEI Number
1450392
Entity Name
NORFOLK MEDICAL PRODUCTS, INC.
City/State/Country
Skokie, IL, US
Establishment Address
7350 NORTH RIDGEWAY, Skokie, IL 60076, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
NORFOLK MEDICAL PRODUCTS, INC. (Owner Number: 1450392)
Owner / Operator Contact Address
7350 NORTH RIDGEWAY, --, Skokie, IL 60076, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K102385
PMA Number
N/A

All Registered Proprietary Names

POSI GRIP NEEDLE ClearView Set/ClearView-MS Set/Aqua-C Hydration System Clear-View Set NorPort TidalPort Norport

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GAA Needle, Aspiration And Injection, Disposable General, Plastic Surgery Class 1 878.4800 1992-09-16
FPA Set, Administration, Intravascular General Hospital Class 2 880.5440 2008-01-17
LJT Port & Catheter, Implanted, Subcutaneous, Intravascular General Hospital Class 2 880.5965 2015-10-05
LJT Port & Catheter, Implanted, Subcutaneous, Intravascular General Hospital Class 2 880.5965 2012-10-09
LJT Port & Catheter, Implanted, Subcutaneous, Intravascular General Hospital Class 2 880.5965 2012-10-09

Official Correspondent

MICHAEL DALTON

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NORFOLK MEDICAL PRODUCTS, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K781371 Ferris Mfg. Corp. BONE MARROW ASPIRATION KIT 1978-09-20
K221518 Np Medical NP Medical nCompass Extension Set with Stabilizing Base 2022-11-03
K953474 Medikmark, Inc. IV START KIT 1995-10-02
K972493 Nipro Medical Corp. NIPRO DISPOSABLE SOLUTION INFUSION SET 1997-09-18
K982672 Baxter Healthcare Corp COLLEAGUE PUMP SYRINGE ADAPTER SET 1998-09-04

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0017-2023 Hobbs Medical, Inc. 1
Hobbs Transbronchial Aspiration Needle and Vacu-lok Aspirating Syringe Catalog Number: 4620
Z-0018-2023 Hobbs Medical, Inc. 1
Hobbs Transbronchial Aspiration Needle Catalog Number: 4621
Z-0023-2011 Becton Dickinson & Company 1
BD 30G1/2 PrecisionGlide Needle;Catalog/Lot Number: 305106. Needles are intended for use in aspiration and injection of medications.
Z-0010-2025 Smiths Medical ASD Inc. 2
CADD Medication Cassette Reservoir, 100mL, Product Code 21-7002-24
Z-0011-2025 Smiths Medical ASD Inc. 2
CADD Medication Cassette Reservoir, 100mL, FS, Product Code 21-7302-24

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1450392. Last updated year: 2026. Please use registration number 1450392 when referencing this establishment in official correspondence.
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