UROVIEW— 510(k) K872022

Substantially Equivalent

Oec-Diasonics, Inc.

FDA 510(k) clearance K872022 for UROVIEW, Substantially Equivalent on 1987-07-16. Applicant: Oec-Diasonics, Inc..

Clearance details

Applicant: Oec-Diasonics, Inc.
Product code: Code KQS
Advisory panel: Gastroenterology, Urology
Date received: 1987-05-26
Decision date: 1987-07-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

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