VIBRALUNG ACOUSTICAL PERCUSSOR— 510(k) K133057

Substantially Equivalent

Westmed, Inc.

FDA 510(k) clearance K133057 for VIBRALUNG ACOUSTICAL PERCUSSOR, Substantially Equivalent on 2014-05-23. Applicant: Westmed, Inc.. Device class: 2.

Clearance details

Applicant: Westmed, Inc.
Product code: Code SDT
Device class: Class 2
Regulation: 21 CFR 868.5665
Advisory panel: Anesthesiology
Date received: 2013-09-27
Decision date: 2014-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tucson, AZ, 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.