ANGIOSCOPY CATHETER— 510(k) K832698

Substantially Equivalent

American Edwards Laboratories

FDA 510(k) clearance K832698 for ANGIOSCOPY CATHETER, Substantially Equivalent on 1983-11-03. Applicant: American Edwards Laboratories.

Clearance details

Applicant: American Edwards Laboratories
Product code: Code LYK
Advisory panel: Gastroenterology, Urology
Date received: 1983-08-10
Decision date: 1983-11-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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