F.M. WEIST,KG (URODYNAMIC SYSTEMS)— 510(k) K860571

Name: FDA 510(k) clearance K860571
Creator: U.S. Food and Drug Administration
Published: 1986-03-18

Substantially Equivalent

F.M. Wiest USA, Inc.

FDA 510(k) clearance K860571 for F.M. WEIST,KG (URODYNAMIC SYSTEMS), Substantially Equivalent on 1986-03-18. 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: 1986-02-14
Decision date: 1986-03-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cherry Hill, NJ, US

Download summary PDF View on FDA.gov ↗

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