Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K033264
Device Classification Name
Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
More FDA Info for this Device
510(K) Number
K033264
Device Name
Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Applicant
MEDTRONIC PERFUSION SYSTEMS
7611 NORTHLAND DR.
MINNEAPOLIS, MN 55038 US
Other 510(k) Applications for this Company
Contact
PREETI JAIN
Other 510(k) Applications for this Contact
Regulation Number
870.4210
More FDA Info for this Regulation Number
Classification Product Code
DWF
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
10/09/2003
Decision Date
10/31/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact