FDA 510(k) Application Details - K133659

Device Classification Name	Automated External Defibrillators (Non-Wearable)   More FDA Info for this Device
510(K) Number	K133659
Device Name	Automated External Defibrillators (Non-Wearable)
Applicant	PHILIPS MEDICAL SYSTEMS 22100 BOTHELL EVERETT WAY BOTHELL, WA 98021 US Other 510(k) Applications for this Company
Contact	JOHN PARDO Other 510(k) Applications for this Contact
Regulation Number	870.5310   More FDA Info for this Regulation Number
Classification Product Code	MKJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/27/2013
Decision Date	01/23/2015
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