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FDA 510(k)

PROTECT-AIDS AUTOPSY UNDERGLOVE

K-Number: K880440 · 1988-10-11

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

Device Summary

PROTECT-AIDS AUTOPSY 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 K880440. 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 AUTOPSY UNDERGLOVE?

PROTECT-AIDS AUTOPSY 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 K880440.

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

PROTECT-AIDS AUTOPSY UNDERGLOVE received FDA 510(k) clearance on 1988-10-11, under 510(k) number K880440.

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

The FDA product code for PROTECT-AIDS AUTOPSY 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.

K923229MEDARMOR FINGER TIP, PUNCTURE RESISTANT UNDERGLOVEK912737MEDARMOR FINGERTIP, PUNC/CUT RESIST SURG EXAM GLOVK912457MEDARMOR FINGERTIP, PUNCTURE AND CUT RESISTANT GLOK880439PROTECT-AIDS 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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