VIMOVE— 510(k) K131094

Substantially Equivalent

Dorsa VI Pty., Ltd.

FDA 510(k) clearance K131094 for VIMOVE, Substantially Equivalent on 2014-07-11. Applicant: Dorsa VI Pty., Ltd.. Device class: 2.

Clearance details

Applicant: Dorsa VI Pty., Ltd.
Product code: Code IKN
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 2013-04-18
Decision date: 2014-07-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chalotte, NC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IKN

K172743 — Natus VikingQuest2017-12-19
K163150 — ViMove22017-07-14
K162383 — Cadwell Sierra Summit, Cadwell Sierra Ascent2017-03-01
K142494 — ViMove2015-05-28
K123902 — PHYSICAL MONITORING REGISTRATION UNIT-S (PMRU-S)2013-09-13

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