FDA 510(k) Application Details - K963910

Device Classification Name	Nebulizer (Direct Patient Interface)   More FDA Info for this Device
510(K) Number	K963910
Device Name	Nebulizer (Direct Patient Interface)
Applicant	VORTRAN MEDICAL TECHNOLOGY 1, INC. 3941 J ST., SUITE 354 SACRAMENTO, CA 95819 US Other 510(k) Applications for this Company
Contact	GORDON A WONG 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	09/30/1996
Decision Date	12/16/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review