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FDA 510(k)

CUT RESISTANT GLOVE LINER

K-Number: K902633 · 1990-07-27

ApplicantBiomet, Inc.
Decision Date1990-07-27
Product CodeLYU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CUT RESISTANT GLOVE LINER is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 1990-07-27 under 510(k) number K902633. 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 CUT RESISTANT GLOVE LINER?

CUT RESISTANT GLOVE LINER is a medical device that received FDA 510(k) clearance on 1990-07-27. The listed applicant is Biomet, Inc.. The 510(k) number is K902633.

When did CUT RESISTANT GLOVE LINER receive FDA 510(k) clearance?

CUT RESISTANT GLOVE LINER received FDA 510(k) clearance on 1990-07-27, under 510(k) number K902633.

Who is the listed applicant for CUT RESISTANT GLOVE LINER?

The FDA 510(k) record lists Biomet, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CUT RESISTANT GLOVE LINER?

The FDA product code for CUT RESISTANT GLOVE LINER is LYU.

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Related Devices (Code: LYU)

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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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