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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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