AMBIDERM(TM) PATIENT EXAMINATION GLOVE (LATEX)— 510(k) K891298

Substantially Equivalent

Medi Tex, Inc.

FDA 510(k) clearance K891298 for AMBIDERM(TM) PATIENT EXAMINATION GLOVE (LATEX), Substantially Equivalent on 1989-03-29. Applicant: Medi Tex, Inc..

Clearance details

Applicant: Medi Tex, Inc.
Product code: Code LYY
Advisory panel: General Hospital
Date received: 1989-03-13
Decision date: 1989-03-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

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