MERKUR 4000— 510(k) K920575

Substantially Equivalent

F.M. Wiest USA, Inc.

FDA 510(k) clearance K920575 for MERKUR 4000, Substantially Equivalent on 1992-07-23. Applicant: F.M. Wiest USA, Inc.. Device class: 2.

Clearance details

Applicant: F.M. Wiest USA, Inc.
Product code: Code FAP
Device class: Class 2
Regulation: 21 CFR 876.1620
Advisory panel: Gastroenterology, Urology
Date received: 1992-02-07
Decision date: 1992-07-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oradell, NJ, US

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