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Diabetic Needle Disposal, Model # PMSM - 950

FDA 510(k)

Class II (US FDA 510(k))

510(k) K990371

by Post Medical, Inc.

Identifiers

510(k) Number
K990371 FDA 510(k)
FDA Product Code
FMI FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 880.5570 FDA 510(k)
Regulation Number
880.5570 FDA 510(k)
Advisory Committee
General Hospital FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

The Diabetic Needle Disposal, Model # PMSM - 950 is a needle, hypodermic, single lumen device. It is intended for use by diabetic patients at home for the collection of contaminated disposable sharps at the point of use.

This device is supplied by Post Medical, Inc. and has received FDA 510(k) clearance. It is classified as a Class II device under product code FMI.

Frequently asked questions

What is the intended use of the PMSM-950 device?

This device is specifically intended for use by diabetic patients in a home setting. It serves as a collection container for contaminated disposable sharps at the point of use to ensure safe disposal.

Is this device cleared for use by regulatory bodies?

Yes, the Diabetic Needle Disposal, Model PMSM-950, has received FDA 510(k) clearance. It is classified as a Class II device under product code FMI.

Who is the manufacturer of this needle disposal device?

The device is supplied by Post Medical, Inc., located in Atlanta, Georgia. The company received clearance for this specific model under K-number K990371.

This description and any FAQs above were generated automatically from registry data and have not been verified by the manufacturer or by deviCERTS. Always check the official registry entry and the manufacturer's instructions for use before relying on them. Sources consulted: DIABETIC NEEDLE DISPOSAL, MODEL # PMSM - 950 (K990371) — FDA 510 (k ..., K990371 FDA 510 (k) - DIABETIC NEEDLE DISPOSAL, Diabetic Needle Disposal, Model # Pmsm - 950 510 (k) FDA Premarket ..., K990371 FDA 510 (k) - DIABETIC NEEDLE DISPOSAL, Post Medical, Inc. PMSM-950 GUDID Device - FDA.report

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

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Manufacturer

Manufacturer
Post Medical, Inc.

Sources (1)

  • FDA 510(k) K990371 24 fields · synced Sep 23, 2026