ANSELL NO POWDER AMBI PATIENT EXAMINATION GLOVES— 510(k) K913766

Substantially Equivalent

Ansell, Inc.

FDA 510(k) clearance K913766 for ANSELL NO POWDER AMBI PATIENT EXAMINATION GLOVES, Substantially Equivalent on 1993-03-11. Applicant: Ansell, Inc..

Clearance details

Applicant: Ansell, Inc.
Product code: Code LYY
Advisory panel: General Hospital
Date received: 1991-08-22
Decision date: 1993-03-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Thailand, TH

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