ViMove— 510(k) K142494

Substantially Equivalent

Dorsavi, Ltd.

FDA 510(k) clearance K142494 for ViMove, Substantially Equivalent on 2015-05-28. Applicant: Dorsavi, Ltd.. Device class: 2.

Clearance details

Applicant: Dorsavi, Ltd.
Product code: Code IKN
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 2014-09-05
Decision date: 2015-05-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: East Melbourne, AU

Download summary PDF View on FDA.gov ↗

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