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FDA 510(k)

PATIENT EXAMINATION GLOVES (NON STERILE)

K-Number: K895657 · 1989-12-11

Decision Date1989-12-11
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT EXAMINATION GLOVES (NON STERILE) is the device name listed in this FDA 510(k) record. The listed applicant is Ka Hung Development , Ltd.. It received FDA 510(k) clearance on 1989-12-11 under 510(k) number K895657. 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 GLOVES (NON STERILE)?

PATIENT EXAMINATION GLOVES (NON STERILE) is a medical device that received FDA 510(k) clearance on 1989-12-11. The listed applicant is Ka Hung Development , Ltd.. The 510(k) number is K895657.

When did PATIENT EXAMINATION GLOVES (NON STERILE) receive FDA 510(k) clearance?

PATIENT EXAMINATION GLOVES (NON STERILE) received FDA 510(k) clearance on 1989-12-11, under 510(k) number K895657.

Who is the listed applicant for PATIENT EXAMINATION GLOVES (NON STERILE)?

The FDA 510(k) record lists Ka Hung Development , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PATIENT EXAMINATION GLOVES (NON STERILE)?

The FDA product code for PATIENT EXAMINATION GLOVES (NON STERILE) is LYY.

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.

Related Devices (Code: LYY)

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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