FDA 510(k) Application Details - K010565

Device Classification Name	Interferential Current Therapy   More FDA Info for this Device
510(K) Number	K010565
Device Name	Interferential Current Therapy
Applicant	DYNATRONICS CORP. 7030 PARK CENTRE DR. SALT LAKE CITY, UT 84121 US Other 510(k) Applications for this Company
Contact	JOHN S RAMEY Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LIH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/26/2001
Decision Date	05/15/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review