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FDA 510(k)

MEDARMOR FINGER TIP, PUNCTURE RESISTANT UNDERGLOVE

K-Number: K923229 · 1993-05-07

ApplicantMedical Armor Corp.
Decision Date1993-05-07
Product CodeLYU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDARMOR FINGER TIP, PUNCTURE RESISTANT UNDERGLOVE 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 1993-05-07 under 510(k) number K923229. 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 FINGER TIP, PUNCTURE RESISTANT UNDERGLOVE?

MEDARMOR FINGER TIP, PUNCTURE RESISTANT UNDERGLOVE is a medical device that received FDA 510(k) clearance on 1993-05-07. The listed applicant is Medical Armor Corp.. The 510(k) number is K923229.

When did MEDARMOR FINGER TIP, PUNCTURE RESISTANT UNDERGLOVE receive FDA 510(k) clearance?

MEDARMOR FINGER TIP, PUNCTURE RESISTANT UNDERGLOVE received FDA 510(k) clearance on 1993-05-07, under 510(k) number K923229.

Who is the listed applicant for MEDARMOR FINGER TIP, PUNCTURE RESISTANT UNDERGLOVE?

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 FINGER TIP, PUNCTURE RESISTANT UNDERGLOVE?

The FDA product code for MEDARMOR FINGER TIP, PUNCTURE RESISTANT UNDERGLOVE is LYU.

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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.

K912737MEDARMOR FINGERTIP, PUNC/CUT RESIST SURG EXAM GLOVK912457MEDARMOR 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.

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