FDA 510(k) Application Details - K033710

Device Classification Name	Humidifier, Respiratory Gas, (Direct Patient Interface)   More FDA Info for this Device
510(K) Number	K033710
Device Name	Humidifier, Respiratory Gas, (Direct Patient Interface)
Applicant	FISHER & PAYKEL HEALTHCARE, LTD. P.O BOX 14-348 PANMURE, AUCKLAND 1701 NZ Other 510(k) Applications for this Company
Contact	BRETT WHISTON Other 510(k) Applications for this Contact
Regulation Number	868.5450   More FDA Info for this Regulation Number
Classification Product Code	BTT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/26/2003
Decision Date	04/13/2004
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