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FDA 510(k)

LOCK-UP

K-Number: K951736 · 1995-07-05

ApplicantMedline
Decision Date1995-07-05
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LOCK-UP is the device name listed in this FDA 510(k) record. The listed applicant is Medline. It received FDA 510(k) clearance on 1995-07-05 under 510(k) number K951736. 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 LOCK-UP?

LOCK-UP is a medical device that received FDA 510(k) clearance on 1995-07-05. The listed applicant is Medline. The 510(k) number is K951736.

When did LOCK-UP receive FDA 510(k) clearance?

LOCK-UP received FDA 510(k) clearance on 1995-07-05, under 510(k) number K951736.

Who is the listed applicant for LOCK-UP?

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

What is the FDA product code for LOCK-UP?

The FDA product code for LOCK-UP is FMI.

Other records listing Medline 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.

K120156PUREIMAGE ULTRASOUND TRANSMISSION GELK051378POWDER-FREE BLUE NITRILE EXAMINATION GLOVES (TESTED FOR USE WITH CHEMOTHERAPY DRUGS)K010825MEDLINE STERISET STERILIZATION CONTAINERK990463MEDLINE EXCEL WHEELCHAIRSK970282MEDLINE CIRCUMCISION TRAYK963504MEDLINE OPEN END FINGER CONTROL MITT

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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

View on FDA Database →

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

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