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FDA 510(k)

LI WAH LATEX EXAMINATION GLOVES

K-Number: K891323 · 1989-08-31

ApplicantLi Wah-Hong Kong, Inc.
Decision Date1989-08-31
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LI WAH LATEX EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Li Wah-Hong Kong, Inc.. It received FDA 510(k) clearance on 1989-08-31 under 510(k) number K891323. 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 LI WAH LATEX EXAMINATION GLOVES?

LI WAH LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-08-31. The listed applicant is Li Wah-Hong Kong, Inc.. The 510(k) number is K891323.

When did LI WAH LATEX EXAMINATION GLOVES receive FDA 510(k) clearance?

LI WAH LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1989-08-31, under 510(k) number K891323.

Who is the listed applicant for LI WAH LATEX EXAMINATION GLOVES?

The FDA 510(k) record lists Li Wah-Hong Kong, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LI WAH LATEX EXAMINATION GLOVES?

The FDA product code for LI WAH LATEX EXAMINATION GLOVES is LYY.

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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.

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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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