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FDA 510(k)

PROTECT-AIDS UNDERGLOVE

K-Number: K880439 · 1988-10-11

ApplicantMedical Armor Corp.
Decision Date1988-10-11
Product CodeLYU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PROTECT-AIDS 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 1988-10-11 under 510(k) number K880439. 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 PROTECT-AIDS UNDERGLOVE?

PROTECT-AIDS UNDERGLOVE is a medical device that received FDA 510(k) clearance on 1988-10-11. The listed applicant is Medical Armor Corp.. The 510(k) number is K880439.

When did PROTECT-AIDS UNDERGLOVE receive FDA 510(k) clearance?

PROTECT-AIDS UNDERGLOVE received FDA 510(k) clearance on 1988-10-11, under 510(k) number K880439.

Who is the listed applicant for PROTECT-AIDS 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 PROTECT-AIDS UNDERGLOVE?

The FDA product code for PROTECT-AIDS UNDERGLOVE 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.

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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.

K923229MEDARMOR FINGER TIP, PUNCTURE RESISTANT UNDERGLOVEK912737MEDARMOR FINGERTIP, PUNC/CUT RESIST SURG EXAM GLOVK912457MEDARMOR FINGERTIP, PUNCTURE AND CUT RESISTANT GLOK880440PROTECT-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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