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FDA 510(k)

PATIENT EXAMINATION GLOVE (LATEX)

K-Number: K892096 · 1989-04-25

ApplicantGrand Universe Trading Co., Ltd.
Decision Date1989-04-25
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT EXAMINATION GLOVE (LATEX) is the device name listed in this FDA 510(k) record. The listed applicant is Grand Universe Trading Co., Ltd.. It received FDA 510(k) clearance on 1989-04-25 under 510(k) number K892096. 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 PATIENT EXAMINATION GLOVE (LATEX)?

PATIENT EXAMINATION GLOVE (LATEX) is a medical device that received FDA 510(k) clearance on 1989-04-25. The listed applicant is Grand Universe Trading Co., Ltd.. The 510(k) number is K892096.

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

PATIENT EXAMINATION GLOVE (LATEX) received FDA 510(k) clearance on 1989-04-25, under 510(k) number K892096.

Who is the listed applicant for PATIENT EXAMINATION GLOVE (LATEX)?

The FDA 510(k) record lists Grand Universe Trading Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

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

The FDA product code for PATIENT EXAMINATION 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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