FDA 510(k) Application Details - K970298

Device Classification Name	Recorder, Magnetic Tape, Medical   More FDA Info for this Device
510(K) Number	K970298
Device Name	Recorder, Magnetic Tape, Medical
Applicant	DIAGNOSTIC MONITORING 2101 EAST 4TH ST., BLDG. B#270 SANTA ANA, CA 92705 US Other 510(k) Applications for this Company
Contact	RAYMOND COHEN 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	01/27/1997
Decision Date	08/20/1997
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