ANGIOSCOPE— 510(k) K830084

Substantially Equivalent

Trimedyne, Inc.

FDA 510(k) clearance K830084 for ANGIOSCOPE, Substantially Equivalent on 1983-06-02. Applicant: Trimedyne, Inc..

Clearance details

Applicant: Trimedyne, Inc.
Product code: Code LYK
Advisory panel: Gastroenterology, Urology
Date received: 1983-01-11
Decision date: 1983-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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