FDA 510(k) Application Details - K092947

Device Classification Name	Detector And Alarm, Arrhythmia   More FDA Info for this Device
510(K) Number	K092947
Device Name	Detector And Alarm, Arrhythmia
Applicant	SCOTTCARE CORPORATION 4791 WEST 150TH ST. CLEVELAND, OH 44135 US Other 510(k) Applications for this Company
Contact	TIMOTHY J LEYVA 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	09/24/2009
Decision Date	02/26/2010
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