PATIENT EXAMINATION GLOVES (NON STERILE)
K-Number: K895657 · 1989-12-11
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Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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