FDA 510(k) Application Details - K982043

Device Classification Name	Nebulizer (Direct Patient Interface)   More FDA Info for this Device
510(K) Number	K982043
Device Name	Nebulizer (Direct Patient Interface)
Applicant	BREMED ITALIA, S.R.L. 1337 ROCKWOOD FOREST DR. ARNOLD, MO 63010 US Other 510(k) Applications for this Company
Contact	MARK HEBENSTREIT 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	06/10/1998
Decision Date	11/09/1998
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