DYNATRON 350 EMG/BIOFEEDBACK ANALYZER— 510(k) K900639

Name: FDA 510(k) clearance K900639
Creator: U.S. Food and Drug Administration
Published: 1990-10-04

Substantially Equivalent

Dynatronics Laser Corp.

FDA 510(k) clearance K900639 for DYNATRON 350 EMG/BIOFEEDBACK ANALYZER, Substantially Equivalent on 1990-10-04. Applicant: Dynatronics Laser Corp.. Device class: 2.

Clearance details

Applicant: Dynatronics Laser Corp.
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 1990-02-09
Decision date: 1990-10-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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