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

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..

Clearance details

Applicant: Dynatronics Laser Corp.
Product code: Code HCC
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

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