FDA 510(k) Application Details - K030382

Device Classification Name	Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat   More FDA Info for this Device
510(K) Number	K030382
Device Name	Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat
Applicant	SELICOR, INC. 7000 NORTH MOPAC, SECOND FLR. AUSTIN, TX 78731 US Other 510(k) Applications for this Company
Contact	JAMES B BINGHAM Other 510(k) Applications for this Contact
Regulation Number	890.5290   More FDA Info for this Regulation Number
Classification Product Code	IMJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/05/2003
Decision Date	04/01/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review