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FDA 510(k)

LOK-ON NEEDLE DISPOSAL CONTAINER

K-Number: K942624 · 1994-08-25

ApplicantMedical Safety Products, Inc.
Decision Date1994-08-25
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LOK-ON NEEDLE DISPOSAL CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Safety Products, Inc.. It received FDA 510(k) clearance on 1994-08-25 under 510(k) number K942624. 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 LOK-ON NEEDLE DISPOSAL CONTAINER?

LOK-ON NEEDLE DISPOSAL CONTAINER is a medical device that received FDA 510(k) clearance on 1994-08-25. The listed applicant is Medical Safety Products, Inc.. The 510(k) number is K942624.

When did LOK-ON NEEDLE DISPOSAL CONTAINER receive FDA 510(k) clearance?

LOK-ON NEEDLE DISPOSAL CONTAINER received FDA 510(k) clearance on 1994-08-25, under 510(k) number K942624.

Who is the listed applicant for LOK-ON NEEDLE DISPOSAL CONTAINER?

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

What is the FDA product code for LOK-ON NEEDLE DISPOSAL CONTAINER?

The FDA product code for LOK-ON NEEDLE DISPOSAL CONTAINER 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 Medical Safety Products, 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.

K913329V-ACCI-GUARD(TM) REUSABLE HOLDERK895075ACCI-GUARD REUSABLE HOLDERK890751ACCI-GUARD(TM) I.V. CATHETER PLACEMENT UNITK884139ACCI-GUARD(TM) REGULAR AND PEDIATRIC HOLDERK881654ACCI-GUARD MULTI-SAMPLE BLOOD COLLECTION NEEDLE

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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