FDA 510(k) Application Details - DEN080009

Device Classification Name	More FDA Info for this Device
510(K) Number	DEN080009
Device Name	AIRPURGE
Applicant	ANESTHESIA SAFETY PRODUCTS, LLC 155-M NEW BOSTON STREET SUITE 127 WOBURN, MA 01801 US Other 510(k) Applications for this Company
Contact	IHSAN A HADDAD Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OKL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/29/2008
Decision Date	03/04/2014
Decision	DENG -
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status
Type	Post-NSE
Reviewed By Third Party	N
Expedited Review