ViMove2— 510(k) K163150

Substantially Equivalent

Dorsavi, Ltd.

FDA 510(k) clearance K163150 for ViMove2, Substantially Equivalent on 2017-07-14. 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: 2016-11-09
Decision date: 2017-07-14
Decision: Substantially Equivalent
Clearance type: Special
Location: East Melbourne, AU

Download summary PDF View on FDA.gov ↗

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K142494 — ViMove2015-05-28
K131094 — VIMOVE2014-07-11
K123902 — PHYSICAL MONITORING REGISTRATION UNIT-S (PMRU-S)2013-09-13

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