PRIMA CARE MEDICAL SUPPLIES, INC.

FDA Device Registration & Listing · Paterson, NJ, US · Registration 3005616800

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
3005616800
FEI Number
3005616800
Entity Name
PRIMA CARE MEDICAL SUPPLIES, INC.
City/State/Country
Paterson, NJ, US
Establishment Address
239 6th Ave, Paterson, NJ 07524, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Prima-Care Medical Supplies, Inc. (Owner Number: 10039985)
Owner / Operator Contact Address
2401 East Linden Avenue, Linden, NJ 07036, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K082208
PMA Number
N/A

All Registered Proprietary Names

SPHYGMOMANOMETER ANEROID Dressing

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LDE Stethoscope, Manual Cardiovascular Class 1 870.1875 2023-09-08
DXQ Blood Pressure Cuff Cardiovascular Class 2 870.1120 2023-09-08
NAC Dressing, Wound, Hydrophilic General, Plastic Surgery Class 1 878.4018 2013-03-11

Official Correspondent

Joseph Templer

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Prima-Care Medical Supplies, 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
K831001 Frontier Products UNICUFF-BLOOD PRESSURE CUFF 1983-07-28
K253089 Shenzhen Best Electronics Co., Ltd. NIBP Cuff (BCS-112, BCS-212, BCS-312, BCS-412, BCS-512, BCS-612, BCS-712, BCS-122, BCS-222, BCS-322, BCS-422, BCS-522, BCS-622, BCS-722, BCD-112, BCD-212, BCD-312, BCD-412, BCD-512, BCD-612, BCD-712, BCD-122, BCD-222, BCD-322, BCD-422, BCD-522, BCD-622, BCD-722) 2026-02-13
K972301 Rudolf Riester GmbH & Co. KG BIG BEN SQUARE, BIG BEN ROUND 1997-09-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005616800. Last updated year: 2026. Please use registration number 3005616800 when referencing this establishment in official correspondence.
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