DURAPRO (PATIENT EXAMINATION GLOVES)— 510(k) K892130

Substantially Equivalent

Perfekta Intl., Ltd.

FDA 510(k) clearance K892130 for DURAPRO (PATIENT EXAMINATION GLOVES), Substantially Equivalent on 1989-05-31. Applicant: Perfekta Intl., Ltd..

Clearance details

Applicant: Perfekta Intl., Ltd.
Product code: Code LYY
Advisory panel: General Hospital
Date received: 1989-04-04
Decision date: 1989-05-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kowloon, Hong Kong, HK

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