FDA 510(k) Application Details - K832828

Device Classification Name	System, Signal Isolation   More FDA Info for this Device
510(K) Number	K832828
Device Name	System, Signal Isolation
Applicant	CLINICAL DATA INSTRUMENTS, INC. Other 510(k) Applications for this Company
Regulation Number	870.2600   More FDA Info for this Regulation Number
Classification Product Code	DRJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/19/1983
Decision Date	05/09/1984
Decision	SE - Substantially Equivalent
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status
Type	Traditional
Reviewed By Third Party	N
Expedited Review