Medical Device Manufacturer · US , Washington , DC

Dynatronics Corp. - FDA 510(k) Cleared Devices

24 submissions · 19 cleared · Since 1987

Recent clearances: DYNATRON PELTIER THERMOSTIM PROBE, DYNATRON TRI-WAVE LIGHT PAD DYNATRON TRI-WAVE LIGHT PROBE, DYNATRON ION IONTOPHORESIS ELECTRODE

24

Total

19

Cleared

0

Denied

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

10 devices

1-10 of 10

Cleared Jan 24, 2014

DYNATRON PELTIER THERMOSTIM PROBE

Neurology · 205d

Cleared May 15, 2001

Neurology · 78d

Cleared May 15, 2001

DYNATRON STS RX

Neurology · 47d

Cleared Sep 05, 1996

Neurology · 156d

Cleared Sep 13, 1995

Neurology · 229d

Cleared Sep 13, 1995

Neurology · 229d

Cleared Sep 01, 1995

Neurology · 519d

Cleared Jan 14, 1993

Neurology · 154d

Cleared Mar 15, 1991

DYNATRON 200 MICROCURRENT

Neurology · 219d

Cleared Apr 18, 1990

DYNATRON 360 RANGE OF MOTION TESTING DEVICE

Neurology · 112d