FDA 510(k) Applications Submitted by RON HATCH

FDA 510(k) Number Submission Date Device Name Applicant
K040729 03/22/2004 SOLARIS D890 THERAPY PROBE DYNATRONICS CORP.
K031329 04/28/2003 DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE (OPTIONAL ACCESSORY) DYNATRONICS CORP.
K051680 06/23/2005 DYNATRON DX2 TRACTION UNIT DYNATRONICS CORP.
K051261 05/16/2005 DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBE DYNATRONICS CORP.
K043047 11/04/2004 DYNATRON IBOX IONTOPHORESIS DEVICE DYNATRONICS CORP.


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