FDA 510(k) Application Details - K101022

Device Classification Name	Recorder, Magnetic Tape, Medical   More FDA Info for this Device
510(K) Number	K101022
Device Name	Recorder, Magnetic Tape, Medical
Applicant	KARMELSONIX 31 HAAVODA ST. BINYAMINA IL Other 510(k) Applications for this Company
Contact	YORAM LEVY Other 510(k) Applications for this Contact
Regulation Number	870.2800   More FDA Info for this Regulation Number
Classification Product Code	DSH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/13/2010
Decision Date	07/09/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review