FDA 510(k) Application Details - K960446

Device Classification Name	Cable, Transducer And Electrode, Patient, (Including Connector)   More FDA Info for this Device
510(K) Number	K960446
Device Name	Cable, Transducer And Electrode, Patient, (Including Connector)
Applicant	MEDTRONIC VASCULAR 7000 CENTRAL AVE. NE MINNEAPOLIS, MN 55432-3576 US Other 510(k) Applications for this Company
Contact	VALERIE K STUHR Other 510(k) Applications for this Contact
Regulation Number	870.2900   More FDA Info for this Regulation Number
Classification Product Code	DSA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/01/1996
Decision Date	05/22/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review