FDA 510(k) Application Details - K133951

Device Classification Name	Nebulizer (Direct Patient Interface)   More FDA Info for this Device
510(K) Number	K133951
Device Name	Nebulizer (Direct Patient Interface)
Applicant	NEXUS6, LTD. 8 COMMERCE STREET SUITE 205 AUCKLAND 1010 NZ Other 510(k) Applications for this Company
Contact	GARTH SUTHERLAND 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	12/23/2013
Decision Date	04/25/2014
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	N
Expedited Review