Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MEDARMOR FINGERTIP, PUNC/CUT RESIST SURG EXAM GLOV

K-Number: K912737 · 1991-10-08

ApplicantMedical Armor Corp.
Decision Date1991-10-08
Product CodeLYU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDARMOR FINGERTIP, PUNC/CUT RESIST SURG EXAM GLOV is the device name listed in this FDA 510(k) record. The listed applicant is Medical Armor Corp.. It received FDA 510(k) clearance on 1991-10-08 under 510(k) number K912737. 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 MEDARMOR FINGERTIP, PUNC/CUT RESIST SURG EXAM GLOV?

MEDARMOR FINGERTIP, PUNC/CUT RESIST SURG EXAM GLOV is a medical device that received FDA 510(k) clearance on 1991-10-08. The listed applicant is Medical Armor Corp.. The 510(k) number is K912737.

When did MEDARMOR FINGERTIP, PUNC/CUT RESIST SURG EXAM GLOV receive FDA 510(k) clearance?

MEDARMOR FINGERTIP, PUNC/CUT RESIST SURG EXAM GLOV received FDA 510(k) clearance on 1991-10-08, under 510(k) number K912737.

Who is the listed applicant for MEDARMOR FINGERTIP, PUNC/CUT RESIST SURG EXAM GLOV?

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

What is the FDA product code for MEDARMOR FINGERTIP, PUNC/CUT RESIST SURG EXAM GLOV?

The FDA product code for MEDARMOR FINGERTIP, PUNC/CUT RESIST SURG EXAM GLOV 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 Medical Armor Corp. 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.

K923229MEDARMOR FINGER TIP, PUNCTURE RESISTANT UNDERGLOVEK912457MEDARMOR FINGERTIP, PUNCTURE AND CUT RESISTANT GLOK880439PROTECT-AIDS UNDERGLOVEK880440PROTECT-AIDS AUTOPSY UNDERGLOVE

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.

↑