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FDA 510(k)

REPEL(TM) LITE CUT RESISTANT GLOVE LINERS

K-Number: K914077 · 1991-12-02

ApplicantDepuy-Raynham
Decision Date1991-12-02
Product CodeLYU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

REPEL(TM) LITE CUT RESISTANT GLOVE LINERS is the device name listed in this FDA 510(k) record. The listed applicant is Depuy-Raynham. It received FDA 510(k) clearance on 1991-12-02 under 510(k) number K914077. The device is classified under product code LYU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPEL(TM) LITE CUT RESISTANT GLOVE LINERS?

REPEL(TM) LITE CUT RESISTANT GLOVE LINERS is a medical device that received FDA 510(k) clearance on 1991-12-02. The listed applicant is Depuy-Raynham. The 510(k) number is K914077.

When did REPEL(TM) LITE CUT RESISTANT GLOVE LINERS receive FDA 510(k) clearance?

REPEL(TM) LITE CUT RESISTANT GLOVE LINERS received FDA 510(k) clearance on 1991-12-02, under 510(k) number K914077.

Who is the listed applicant for REPEL(TM) LITE CUT RESISTANT GLOVE LINERS?

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

What is the FDA product code for REPEL(TM) LITE CUT RESISTANT GLOVE LINERS?

The FDA product code for REPEL(TM) LITE CUT RESISTANT GLOVE LINERS is LYU.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Depuy-Raynham 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.

K910941LIFELINER SURGICAL GLOVEK900310REPEL SURGICAL GLOVE LINERS

Related Devices (Code: LYU)

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.

K011755STRYKER T4 HYTREL (R) TOGASStryker Corp.K965237NURSES BOUFFANT CAPCopioumed Intl., Inc.K970988FAR-EAST BOUFFANT CAPSFar East Science & Technology Development Co., Ltd.K964364DISPOSABLE APRONInstrument Makar, Inc.K961791DEPUY DISPOSABLE FILTER/HOODDepuy, Inc.K961454AMMI MAGNI-GUARDAmerican Medical Mfg., Inc.

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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