VESSEL DILATORS— 510(k) K910502

Substantially Equivalent

Akcess Medical Products, Inc.

FDA 510(k) clearance K910502 for VESSEL DILATORS, Substantially Equivalent on 1991-04-29. Applicant: Akcess Medical Products, Inc..

Clearance details

Applicant: Akcess Medical Products, Inc.
Product code: Code FKA
Advisory panel: Gastroenterology, Urology
Date received: 1991-02-05
Decision date: 1991-04-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Brunswick, NJ, US

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