FDA 510(k) Application Details - K014056

Device Classification Name	Nebulizer (Direct Patient Interface)   More FDA Info for this Device
510(K) Number	K014056
Device Name	Nebulizer (Direct Patient Interface)
Applicant	SALTER LABS 100 W. SYCAMORE RD. ARVIN, CA 93203 US Other 510(k) Applications for this Company
Contact	DUANE KAZAL 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	12/10/2001
Decision Date	02/01/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review