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FDA 510(k)

SHIH KUO LATEX EXAM GLOVE

K-Number: K892083 · 1989-09-01

ApplicantBeverly Ent., Inc.
Decision Date1989-09-01
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHIH KUO LATEX EXAM GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Beverly Ent., Inc.. It received FDA 510(k) clearance on 1989-09-01 under 510(k) number K892083. 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 SHIH KUO LATEX EXAM GLOVE?

SHIH KUO LATEX EXAM GLOVE is a medical device that received FDA 510(k) clearance on 1989-09-01. The listed applicant is Beverly Ent., Inc.. The 510(k) number is K892083.

When did SHIH KUO LATEX EXAM GLOVE receive FDA 510(k) clearance?

SHIH KUO LATEX EXAM GLOVE received FDA 510(k) clearance on 1989-09-01, under 510(k) number K892083.

Who is the listed applicant for SHIH KUO LATEX EXAM GLOVE?

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

What is the FDA product code for SHIH KUO LATEX EXAM GLOVE?

The FDA product code for SHIH KUO LATEX EXAM GLOVE is LYY.

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Related Devices (Code: LYY)

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Official Source

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