FDA 510(k) Applications Submitted by DYNATRONICS CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K132057	07/03/2013	DYNATRON PELTIER THERMOSTIM PROBE	DYNATRONICS CORP.
K113250	11/03/2011	DYNATRON TRI-WAVE LIGHT PAD DYNATRON TRI-WAVE LIGHT PROBE	DYNATRONICS CORP.
K010565	02/26/2001	DYNATRON STS	DYNATRONICS CORP.
K010948	03/29/2001	DYNATRON STS RX	DYNATRONICS CORP.
K961250	04/01/1996	DYNATRON 125 ULTRASOUND	DYNATRONICS CORP.
K961261	04/02/1996	DYNATRON 525	DYNATRONICS CORP.
K993919	11/18/1999	DYNATRON 900	DYNATRONICS CORP.
K060814	03/27/2006	DYNATRON ION IONTOPHORESIS ELECTRODE	DYNATRONICS CORP.
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.