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FDA 510(k)

MEDARMOR FINGERTIP, PUNCTURE AND CUT RESISTANT GLO

K-Number: K912457 · 1991-10-04

Decision Date1991-10-04
Product CodeLYU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDARMOR FINGERTIP, PUNCTURE AND CUT RESISTANT GLO 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 1991-10-04 under 510(k) number K912457. 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, PUNCTURE AND CUT RESISTANT GLO?

MEDARMOR FINGERTIP, PUNCTURE AND CUT RESISTANT GLO is a medical device that received FDA 510(k) clearance on 1991-10-04. The listed applicant is Medical Armor Corp.. The 510(k) number is K912457.

When did MEDARMOR FINGERTIP, PUNCTURE AND CUT RESISTANT GLO receive FDA 510(k) clearance?

MEDARMOR FINGERTIP, PUNCTURE AND CUT RESISTANT GLO received FDA 510(k) clearance on 1991-10-04, under 510(k) number K912457.

Who is the listed applicant for MEDARMOR FINGERTIP, PUNCTURE AND CUT RESISTANT GLO?

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, PUNCTURE AND CUT RESISTANT GLO?

The FDA product code for MEDARMOR FINGERTIP, PUNCTURE AND CUT RESISTANT GLO 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.

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.

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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