FDA 510(k) Application Details - K965251

Device Classification Name	Catheter, Percutaneous, Intraspinal, Short Term   More FDA Info for this Device
510(K) Number	K965251
Device Name	Catheter, Percutaneous, Intraspinal, Short Term
Applicant	MEDTRONIC VASCULAR 800 53RD AVENUE, NE P.O. BOX 1250 MINNEAPOLIS, MN 55440-9087 US Other 510(k) Applications for this Company
Contact	PATRICK L JOHNSON Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	MAJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/19/1996
Decision Date	03/18/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review