Medical Device Manufacturer · US , Salt Lake City , UT

Dynatronics Laser Corp. - FDA 510(k) Cleared Devices

5 submissions · 4 cleared · Since 1987

5

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Dynatronics Laser Corp. Neurology ✕

3 devices

1-3 of 3

Cleared Oct 04, 1990

DYNATRON 350 EMG/BIOFEEDBACK ANALYZER

Neurology · 237d

Cleared Mar 08, 1988

Neurology · 34d

Cleared Apr 10, 1987

DYNATRON 1120 EPS (ELECTRICAL POINT STIMULATOR)

Neurology · 156d