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FDA 510(k) Application Details - K072834
Device Classification Name
Clamp, Vascular
More FDA Info for this Device
510(K) Number
K072834
Device Name
Clamp, Vascular
Applicant
SURGICAL INSTRUMENTS BELGIUM SA
220 RIVER RD.
CLAREMONT, NH 03743-5647 US
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Contact
WILLIAM F GREENROSE
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
10/03/2007
Decision Date
01/09/2008
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
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