2K-QDA MOTION/GAIT ANALYSIS SYSTEM— 510(k) K880631

Name: FDA 510(k) clearance K880631
Creator: U.S. Food and Drug Administration
Published: 1988-04-21

Substantially Equivalent

Human Performance Technologies, Inc.

FDA 510(k) clearance K880631 for 2K-QDA MOTION/GAIT ANALYSIS SYSTEM, Substantially Equivalent on 1988-04-21. Applicant: Human Performance Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Human Performance Technologies, Inc.
Product code: Code LXJ
Device class: Class 2
Regulation: 21 CFR 890.5360
Advisory panel: Physical Medicine
Date received: 1988-02-16
Decision date: 1988-04-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: East Setauket, NY, US

Download summary PDF View on FDA.gov ↗

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