FDA 510(k) Application Details - K142960

Device Classification Name	Nebulizer (Direct Patient Interface)   More FDA Info for this Device
510(K) Number	K142960
Device Name	Nebulizer (Direct Patient Interface)
Applicant	Reciprocal Labs 634 W. Main Street, Suite 102 Madison, WI 53703 US Other 510(k) Applications for this Company
Contact	David Hubanks 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	10/14/2014
Decision Date	03/05/2015
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