FDA 510(k) Application Details - K022458

Device Classification Name	Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat   More FDA Info for this Device
510(K) Number	K022458
Device Name	Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat
Applicant	METTLER ELECTRONICS CORP. 1333 SOUTH CLAUDINA ST. ANAHEIM, CA 92805 US Other 510(k) Applications for this Company
Contact	ROBERT E FLEMING 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	07/26/2002
Decision Date	09/26/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review