CAVOMAT— 510(k) K911388

Substantially Equivalent

Wiest USA, Inc.

FDA 510(k) clearance K911388 for CAVOMAT, Substantially Equivalent on 1991-12-04. Applicant: Wiest USA, Inc.. Device class: 2.

Clearance details

Applicant: Wiest USA, Inc.
Product code: Code IKN
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 1991-03-29
Decision date: 1991-12-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Potomac, MD, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.