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FDA 510(k)

SHARPS CONTAINMENT SYSTEM

K-Number: K925816 · 1994-04-29

ApplicantPost Medical, Inc.
Decision Date1994-04-29
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHARPS CONTAINMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Post Medical, Inc.. It received FDA 510(k) clearance on 1994-04-29 under 510(k) number K925816. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHARPS CONTAINMENT SYSTEM?

SHARPS CONTAINMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1994-04-29. The listed applicant is Post Medical, Inc.. The 510(k) number is K925816.

When did SHARPS CONTAINMENT SYSTEM receive FDA 510(k) clearance?

SHARPS CONTAINMENT SYSTEM received FDA 510(k) clearance on 1994-04-29, under 510(k) number K925816.

Who is the listed applicant for SHARPS CONTAINMENT SYSTEM?

The FDA 510(k) record lists Post Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHARPS CONTAINMENT SYSTEM?

The FDA product code for SHARPS CONTAINMENT SYSTEM is FMI.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Post Medical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K990371DIABETIC NEEDLE DISPOSAL, MODEL # PMSM - 950K972536SYRINGE NEEDLE REMOVER (S.N.R.)K925086AUTOMATIC NEEDLE DISCONECT (A.N.D.)K830946MALE EXTERNAL CATHETERK830947SYRINGE/NEEDLE DISPOS-BOX-CUTTER/CRIMPER

Related Devices (Code: FMI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261266MOWANA™ Auto DuoPENTAMASTER MEDIQ SDN BHDK261719Promisemed X-Safety Pen NeedlePromisemed Hangzhou Meditech Co., Ltd.K262427Pen Needle (Ordinary Type I, Safety Type IIA, Safety Type IIB, Safety Type IIIA, Safety Type IIIB, Safety Type IV, Safety Type V, Ordinary Type VIA, Ordinary Type VIB, Ordinary Type VIC, Safety Type VII, Ordinary Type IB, Safety type VIII, Safety Type IX, Safety Type X, Ordinary Type XI, Safety Type XII)Hh Global Technology, Inc.K260933Safety Sterile Hypodermic Needles (NR-S1816R, NR-S1916R, NR-S1925R, NR-S1938R, NR-S2016R, NR-S2025R, NR-S2038R, NR-S2051R, NR-S2116R, NR-S2125R, NR-S2138R, NR-S2151R, NR-S2216R, NR-S2225R, NR-S2238R, NR-S2251R, NR-S2316R, NR-S2325R, NR-S2338R, NR-S2351R, NR-S2516R, NR-S2525R, NR-S2538R, NR-S2551R, NR-S2516T, NR-S2525T, NR-S2538T, NR-S2551T)Hangzhou Qiantang Longyue Biotechnology Co., Ltd.K261829Profoject™ Dual-Safety Pen NeedlesCMT Health PTE., Ltd.K260739Profoject™ Pen Needles (Model A; Model B)CMT Health PTE., Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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