INTEGRATED MOVEMENT ANALYZER— 510(k) K944787

Substantially Equivalent

Maryrose

FDA 510(k) clearance K944787 for INTEGRATED MOVEMENT ANALYZER, Substantially Equivalent on 1995-07-07. Applicant: Maryrose. Device class: 2.

Clearance details

Applicant: Maryrose
Product code: Code IKN
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 1994-09-28
Decision date: 1995-07-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tarzana, CA, 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
K131094 — VIMOVE2014-07-11

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