ClearanceBrief
Company ยท US

Dynatronics Laser Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1987 to 1993. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DSBPlethysmograph, Impedance1
GZJStimulator, Nerve, Transcutaneous, For Pain Relief1
HCCDevice, Biofeedback1
IMGStimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat1
LBBDynamometer, Ac-Powered1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 4, 1993K920939DYNATRON 300 ULRASOUND
Dynatronics Laser Corp.
IMG
Oct 4, 1990K900639DYNATRON 350 EMG/BIOFEEDBACK ANALYZER
Dynatronics Laser Corp.
HCC
Jun 11, 1990K900321DYNATRON 330 BODY COMPOSITION ANALYZER
Dynatronics Laser Corp.
DSB
Mar 8, 1988K880464DYNATRON II
Dynatronics Laser Corp.
LBB
Apr 10, 1987K864370DYNATRON 1120 EPS (ELECTRICAL POINT STIMULATOR)
Dynatronics Laser Corp.
GZJ

Latest recalls

DateFirm and productCodeLinked 510(k)
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