ULTRA-VU ANGIOSCOPE— 510(k) K902329

Substantially Equivalent

Angiolaz, Inc.

FDA 510(k) clearance K902329 for ULTRA-VU ANGIOSCOPE, Substantially Equivalent on 1990-08-22. Applicant: Angiolaz, Inc..

Clearance details

Applicant: Angiolaz, Inc.
Product code: Code LYK
Advisory panel: Gastroenterology, Urology
Date received: 1990-05-24
Decision date: 1990-08-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rockingham, VT, US

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