ACTIS (VENOUS FLOW CONTROLLER)— 510(k) K962915

Substantially Equivalent

Vivus, Inc.

FDA 510(k) clearance K962915 for ACTIS (VENOUS FLOW CONTROLLER), Substantially Equivalent on 1996-12-10. Applicant: Vivus, Inc.. Device class: 2.

Clearance details

Applicant: Vivus, Inc.
Product code: Code LKY
Device class: Class 2
Regulation: 21 CFR 876.5020
Advisory panel: Gastroenterology, Urology
Date received: 1996-07-26
Decision date: 1996-12-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Menlo Park, CA, US

Download summary PDF View on FDA.gov ↗

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