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FDA 510(k)

NEEDLE-SHIELD

K-Number: K900282 · 1990-02-28

ApplicantMacbrud Corp. Medical Div.
Decision Date1990-02-28
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NEEDLE-SHIELD is the device name listed in this FDA 510(k) record. The listed applicant is Macbrud Corp. Medical Div.. It received FDA 510(k) clearance on 1990-02-28 under 510(k) number K900282. 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 NEEDLE-SHIELD?

NEEDLE-SHIELD is a medical device that received FDA 510(k) clearance on 1990-02-28. The listed applicant is Macbrud Corp. Medical Div.. The 510(k) number is K900282.

When did NEEDLE-SHIELD receive FDA 510(k) clearance?

NEEDLE-SHIELD received FDA 510(k) clearance on 1990-02-28, under 510(k) number K900282.

Who is the listed applicant for NEEDLE-SHIELD?

The FDA 510(k) record lists Macbrud Corp. Medical Div. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEEDLE-SHIELD?

The FDA product code for NEEDLE-SHIELD 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 Macbrud Corp. Medical Div. 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.

K913049SLIP-PRUF-CLINGERK911873X-MARXK891090SPECBOARD

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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