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FDA 510(k) Application Details - K062474
Device Classification Name
Clamp, Vascular
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510(K) Number
K062474
Device Name
Clamp, Vascular
Applicant
MCPHERSON ENTERPRISES, INC.
3851 62ND AVE. N.
SUITE A
PINELLAS PARK, FL 33781 US
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Contact
WILLIAM MCPHERSON
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
08/24/2006
Decision Date
11/09/2006
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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