RADVISION— 510(k) K131428

Substantially Equivalent

Acoustic Medsystems, Inc.

FDA 510(k) clearance K131428 for RADVISION, Substantially Equivalent on 2013-07-16. Applicant: Acoustic Medsystems, Inc.. Device class: 2.

Clearance details

Applicant: Acoustic Medsystems, Inc.
Product code: Code MUJ
Device class: Class 2
Regulation: 21 CFR 892.5050
Advisory panel: Radiology
Date received: 2013-05-17
Decision date: 2013-07-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Savoy, IL, US

Download summary PDF View on FDA.gov ↗

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