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FDA 510(k) Application Details - K072167
Device Classification Name
Clamp, Vascular
More FDA Info for this Device
510(K) Number
K072167
Device Name
Clamp, Vascular
Applicant
ADVANCED VASCULAR DYNAMICS
2326 NW EVERETT ST.
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
08/06/2007
Decision Date
09/06/2007
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
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