KNEEKG— 510(k) K091000

Substantially Equivalent

Emovi

FDA 510(k) clearance K091000 for KNEEKG, Substantially Equivalent on 2009-10-26. Applicant: Emovi. Device class: 2.

Clearance details

Applicant: Emovi
Product code: Code LXJ
Device class: Class 2
Regulation: 21 CFR 890.5360
Advisory panel: Physical Medicine
Date received: 2009-04-08
Decision date: 2009-10-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montreal, Quebec, CA

Download summary PDF View on FDA.gov ↗

Recent devices under product code LXJ

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