Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K021608
Device Classification Name
Clamp, Vascular
More FDA Info for this Device
510(K) Number
K021608
Device Name
Clamp, Vascular
Applicant
IMPLANTABLE DEVICES
P.O. BOX 270882
TAMPA, FL 33688 US
Other 510(k) Applications for this Company
Contact
WILLIAM E MCPHERSON
Other 510(k) Applications for this Contact
Regulation Number
870.4450
More FDA Info for this Regulation Number
Classification Product Code
DXC
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
05/16/2002
Decision Date
10/22/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact