FDA 510(k) Application Details - K111408

Device Classification Name	Filter, Bacterial, Breathing-Circuit   More FDA Info for this Device
510(K) Number	K111408
Device Name	Filter, Bacterial, Breathing-Circuit
Applicant	CAREFUSION GERMANY 234 GMBH LEIBNIZSTRASSE 7 HOECHBERG, BAVARIA 97204 DE Other 510(k) Applications for this Company
Contact	ELMAR NIEDERMEYER Other 510(k) Applications for this Contact
Regulation Number	868.5260   More FDA Info for this Regulation Number
Classification Product Code	CAH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/19/2011
Decision Date	10/17/2011
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review