FDA 510(k) Application Details - K052252

Device Classification Name	Set, Administration, Intravascular   More FDA Info for this Device
510(K) Number	K052252
Device Name	Set, Administration, Intravascular
Applicant	B. BRAUN MEDICAL, INC. 901 MARCON BLVD. ALLENTOWN, PA 18109-9341 US Other 510(k) Applications for this Company
Contact	CHRISTINE FORD Other 510(k) Applications for this Contact
Regulation Number	880.5440   More FDA Info for this Regulation Number
Classification Product Code	FPA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/18/2005
Decision Date	11/16/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review