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FDA 510(k) Application Details - K090286
Device Classification Name
Clamp, Vascular
More FDA Info for this Device
510(K) Number
K090286
Device Name
Clamp, Vascular
Applicant
ADVANCED VASCULAR DYNAMICS
1910 NW 23RD PLACE
PORTLAND, OR 97210 US
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Contact
HERBERT J SEMLER
Other 510(k) Applications for this Contact
Regulation Number
870.4450
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Classification Product Code
DXC
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More FDA Info for this Product Code
Date Received
02/05/2009
Decision Date
03/23/2009
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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