FDA 510(k) Application Details - K952912

Device Classification Name	Detector And Alarm, Arrhythmia   More FDA Info for this Device
510(K) Number	K952912
Device Name	Detector And Alarm, Arrhythmia
Applicant	SPACELABS MEDICAL, INC. P.O. BOX 97013 REDMOND, WA 98073-9713 US Other 510(k) Applications for this Company
Contact	RUSS GARRISON Other 510(k) Applications for this Contact
Regulation Number	870.1025   More FDA Info for this Regulation Number
Classification Product Code	DSI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/26/1995
Decision Date	04/02/1997
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