FDA 510(k) Application Details - K961615

Device Classification Name	Port & Catheter, Implanted, Subcutaneous, Intravascular   More FDA Info for this Device
510(K) Number	K961615
Device Name	Port & Catheter, Implanted, Subcutaneous, Intravascular
Applicant	ARROW INTL., INC. 1600 PROVIDENCE HIGHWAY WALPOLE, MA 02081 US Other 510(k) Applications for this Company
Contact	BRADLEY J ENEGREN Other 510(k) Applications for this Contact
Regulation Number	880.5965   More FDA Info for this Regulation Number
Classification Product Code	LJT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/26/1996
Decision Date	07/19/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review