FDA 510(k) Application Details - K062689

Device Classification Name	Nebulizer (Direct Patient Interface)   More FDA Info for this Device
510(K) Number	K062689
Device Name	Nebulizer (Direct Patient Interface)
Applicant	RESPIRONICS LTD. 41 CANFIELD ROAD CEDAR GROVE, NJ 07009 US Other 510(k) Applications for this Company
Contact	Lauren Ziegler Other 510(k) Applications for this Contact
Regulation Number	868.5630   More FDA Info for this Regulation Number
Classification Product Code	CAF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/11/2006
Decision Date	02/16/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	Y
Expedited Review