Dynatronics Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
24
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K132057DYNATRON PELTIER THERMOSTIM PROBEJanuary 24, 2014
K113250DYNATRON TRI-WAVE LIGHT PAD DYNATRON TRI-WAVE LIGHT PROBEFebruary 9, 2012
K060814DYNATRON ION IONTOPHORESIS ELECTRODEJune 14, 2006
K051680DYNATRON DX2 TRACTION UNITOctober 11, 2005
K051261DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBEJuly 25, 2005
K043047DYNATRON IBOX IONTOPHORESIS DEVICEJanuary 7, 2005
K040729SOLARIS D890 THERAPY PROBEJune 2, 2004
K031329DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE (OPTIONAL ACCESSORY)October 22, 2003
K010565DYNATRON STSMay 15, 2001
K010948DYNATRON STS RXMay 15, 2001
K993919DYNATRON 900January 3, 2000
K961261DYNATRON 525September 5, 1996
K961250DYNATRON 125 ULTRASOUNDAugust 26, 1996
K950348DYNATRON 650September 13, 1995
K950349DYNATRON 950September 13, 1995
K941577DYNATRON 550September 1, 1995
K944935DYNATRON 250June 22, 1995
K935728DYNATRON 150April 26, 1994
K932937DYNATRON 800October 8, 1993
K924319DYNATRON 400January 14, 1993