FDA 510(k) Application Details - K092408

Device Classification Name	Aid, Cardiopulmonary Resuscitation   More FDA Info for this Device
510(K) Number	K092408
Device Name	Aid, Cardiopulmonary Resuscitation
Applicant	RAPID RESPONSE SOLUTIONS, LLC 601 WEST 20 STREET HIALEAH, FL 33010 US Other 510(k) Applications for this Company
Contact	JORGE MILAN Other 510(k) Applications for this Contact
Regulation Number	870.5200   More FDA Info for this Regulation Number
Classification Product Code	LIX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/06/2009
Decision Date	10/14/2009
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