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FDA 510(k) Application Details - K024107
Device Classification Name
Clamp, Vascular
More FDA Info for this Device
510(K) Number
K024107
Device Name
Clamp, Vascular
Applicant
RADI MEDICAL SYSTEMS AB
PALMBLADSGATAN 10
UPPSALA S-754 50 SE
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Contact
MATS GRANLUND
Other 510(k) Applications for this Contact
Regulation Number
870.4450
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Classification Product Code
DXC
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/13/2002
Decision Date
12/24/2002
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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