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FDA 510(k)

PROSHIELD GLOVE (LATEX)

K-Number: K891426 · 1989-04-26

ApplicantK & M Resources, Inc.
Decision Date1989-04-26
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PROSHIELD GLOVE (LATEX) is the device name listed in this FDA 510(k) record. The listed applicant is K & M Resources, Inc.. It received FDA 510(k) clearance on 1989-04-26 under 510(k) number K891426. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROSHIELD GLOVE (LATEX)?

PROSHIELD GLOVE (LATEX) is a medical device that received FDA 510(k) clearance on 1989-04-26. The listed applicant is K & M Resources, Inc.. The 510(k) number is K891426.

When did PROSHIELD GLOVE (LATEX) receive FDA 510(k) clearance?

PROSHIELD GLOVE (LATEX) received FDA 510(k) clearance on 1989-04-26, under 510(k) number K891426.

Who is the listed applicant for PROSHIELD GLOVE (LATEX)?

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

What is the FDA product code for PROSHIELD GLOVE (LATEX)?

The FDA product code for PROSHIELD GLOVE (LATEX) is LYY.

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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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