FDA 510(k) Application Details - K984286

Device Classification Name	Automated External Defibrillators (Non-Wearable)   More FDA Info for this Device
510(K) Number	K984286
Device Name	Automated External Defibrillators (Non-Wearable)
Applicant	HEWLETT-PACKARD CO. 2401 FOURTH AVENUE, SUITE 500 SEATTLE, WA 98121 US Other 510(k) Applications for this Company
Contact	WILLIAM D JORDAN 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	12/01/1998
Decision Date	12/17/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review