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FDA 510(k) Application Details - K955742
Device Classification Name
Clamp, Vascular
More FDA Info for this Device
510(K) Number
K955742
Device Name
Clamp, Vascular
Applicant
YOUSEF DANESHVAR
33433 W. SIX MILE RD.
LIVONIA, MI 48152 US
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Contact
Y. DANESHVAR
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
12/19/1995
Decision Date
08/12/1996
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
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