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FDA 510(k) Application Details - K023154
Device Classification Name
Clamp, Vascular
More FDA Info for this Device
510(K) Number
K023154
Device Name
Clamp, Vascular
Applicant
VASCULAR CONTROL SYSTEMS, INC
32236- E PASEO ADELANTO
SAN JUAN CAPISTRANO, CA 92675 US
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Contact
AL MEMMOLO
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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
09/23/2002
Decision Date
12/20/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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