PREFERRED MEDICAL PRODUCTS, LLC

FDA Device Registration & Listing · COPPERHILL, TN, US · Registration 1038913

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
1038913
FEI Number
1038913
Entity Name
PREFERRED MEDICAL PRODUCTS, LLC
City/State/Country
COPPERHILL, TN, US
Establishment Address
191 INDUSTRIAL DR, COPPERHILL, TN 37317, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
PREFERRED MEDICAL PRODUCTS (Owner Number: 1038913)
Owner / Operator Contact Address
191 INDUSTRIAL DR., --, Ducktown, TN 37326, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Equipment Covers Waste Pouch Bag Decanter

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JAA System, X-Ray, Fluoroscopic, Image-Intensified Radiology Class 2 892.1650 2007-12-19
KDC Instrument, Surgical, Disposable General, Plastic Surgery Class 1 878.4800 2017-09-06
KPE Container, I.V. General Hospital Class 2 880.5025 2007-12-19

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PREFERRED MEDICAL PRODUCTS
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
K863853 Superior Medical Products EAZY COVERS 1987-03-06
K953974 Medivision Medical Imaging, Ltd. CAMVISION 1000 1996-09-09
K024012 Ge Oec Medical Systems OEC 9800 E/CV+ DIGITAL MOBILE IMAGING SYSTEM 2003-03-20
K970608 Guidant Cardiac and Vascular Surgery EVT MARKER BOARD 1997-04-21
K203010 Apelem-Dms Group Platinum dRF Imaging System 2021-01-22

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0001-2007 GE OEC Medical Systems, Inc 2
GE 4 inch Anterior Cervical Post, GE Part Number 1006385 or 1006385-NAV, GE Healthcare OEC Medical Systems (an accessory used with the InstaTrak 3500 plus and 9800 C-Arm Navigation systems)
Z-0001-2009 Philips Medical Systems North America Co. Phillips 2
NeuViz Dual Multi-Slice Computed Tomography (CT) Scanner System (software). Whole body x-ray computed tomography scanner which features a continuously rotating tube-detector system and functions according to the fan beam principle. The system software is an interactive program used for x-ray scan control, image reconstruction, and image archive/evaluation. It is intended to produce cross-section images of head and body by computer reconstruction of x-ray transmission data taken at different angles. The function of Time Scan is intended to use in contrast scan include single phase and multi-phase scan, that is according to different density of contrast in vessels or organs between different phase to get necessary information to support doctor's diagnosis.
Z-0004-2010 Ge Healthcare 2
GE OEC 9900 Elite ESP To produce mobile fluoroscopic images of human anatomy.
Z-0005-2010 Ge Healthcare 2
GE OEC 9900 Elite GSP Fluoroscopes To produce mobile fluoroscopic images of human anatomy.
Z-0009-04 Siemens Medical Solutions USA, Inc 2
Urology X-Ray System, Uroskop D1/D2/D3 - Hardware for Motor Drive

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1038913. Last updated year: 2026. Please use registration number 1038913 when referencing this establishment in official correspondence.
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