PATIENT LATEX EXAMINATION GLOVE POWDERED & POWDER FREE, STERILE
K-Number: K992681 · 1999-12-16
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Device Summary
Frequently Asked Questions
What is the PATIENT LATEX EXAMINATION GLOVE POWDERED & POWDER FREE, STERILE?
PATIENT LATEX EXAMINATION GLOVE POWDERED & POWDER FREE, STERILE is a medical device that received FDA 510(k) clearance on 1999-12-16. The listed applicant is Wear Safe Malaysia Sdn. Bhd.. The 510(k) number is K992681.
When did PATIENT LATEX EXAMINATION GLOVE POWDERED & POWDER FREE, STERILE receive FDA 510(k) clearance?
PATIENT LATEX EXAMINATION GLOVE POWDERED & POWDER FREE, STERILE received FDA 510(k) clearance on 1999-12-16, under 510(k) number K992681.
Who is the listed applicant for PATIENT LATEX EXAMINATION GLOVE POWDERED & POWDER FREE, STERILE?
The FDA 510(k) record lists Wear Safe Malaysia Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENT LATEX EXAMINATION GLOVE POWDERED & POWDER FREE, STERILE?
The FDA product code for PATIENT LATEX EXAMINATION GLOVE POWDERED & POWDER FREE, 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.
Other records listing Wear Safe Malaysia Sdn. Bhd. as applicant
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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