CAMSYS 6300— 510(k) K920574

Substantially Equivalent

F.M. Wiest USA, Inc.

FDA 510(k) clearance K920574 for CAMSYS 6300, Substantially Equivalent on 1993-02-17. Applicant: F.M. Wiest USA, Inc.. Device class: 2.

Clearance details

Applicant: F.M. Wiest USA, Inc.
Product code: Code EXQ
Device class: Class 2
Regulation: 21 CFR 876.1620
Advisory panel: Gastroenterology, Urology
Date received: 1992-02-07
Decision date: 1993-02-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oradell, NJ, US

Download summary PDF View on FDA.gov ↗

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