COMFIT BLUE POWDER FREE EXAMINATION GLOVE
K-Number: K934813 · 1994-01-07
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Device Summary
Frequently Asked Questions
What is the COMFIT BLUE POWDER FREE EXAMINATION GLOVE?
COMFIT BLUE POWDER FREE EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1994-01-07. The listed applicant is Wembley Rubber Products (M) Sdn Bhd. The 510(k) number is K934813.
When did COMFIT BLUE POWDER FREE EXAMINATION GLOVE receive FDA 510(k) clearance?
COMFIT BLUE POWDER FREE EXAMINATION GLOVE received FDA 510(k) clearance on 1994-01-07, under 510(k) number K934813.
Who is the listed applicant for COMFIT BLUE POWDER FREE EXAMINATION GLOVE?
The FDA 510(k) record lists Wembley Rubber Products (M) Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COMFIT BLUE POWDER FREE EXAMINATION GLOVE?
The FDA product code for COMFIT BLUE POWDER FREE EXAMINATION GLOVE 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 Wembley Rubber Products (M) 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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