PROFEEL SYNTHETIC COPOLYMER SURGICAL GLOVES (POWDERED)
K-Number: K982600 · 1999-03-12
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Device Summary
Frequently Asked Questions
What is the PROFEEL SYNTHETIC COPOLYMER SURGICAL GLOVES (POWDERED)?
PROFEEL SYNTHETIC COPOLYMER SURGICAL GLOVES (POWDERED) is a medical device that received FDA 510(k) clearance on 1999-03-12. The listed applicant is Wembley Rubber Products (M) Sdn Bhd. The 510(k) number is K982600.
When did PROFEEL SYNTHETIC COPOLYMER SURGICAL GLOVES (POWDERED) receive FDA 510(k) clearance?
PROFEEL SYNTHETIC COPOLYMER SURGICAL GLOVES (POWDERED) received FDA 510(k) clearance on 1999-03-12, under 510(k) number K982600.
Who is the listed applicant for PROFEEL SYNTHETIC COPOLYMER SURGICAL GLOVES (POWDERED)?
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 PROFEEL SYNTHETIC COPOLYMER SURGICAL GLOVES (POWDERED)?
The FDA product code for PROFEEL SYNTHETIC COPOLYMER SURGICAL GLOVES (POWDERED) is KGO.
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: KGO)
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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