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FDA 510(k) Application Details - K022754
Device Classification Name
Clamp, Vascular
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510(K) Number
K022754
Device Name
Clamp, Vascular
Applicant
S & T AG
28438 BALLARD DR.
LAKE FOREST, IL 60045 US
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Contact
BERNHARD TEITZ
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Regulation Number
870.4450
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Classification Product Code
DXC
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Date Received
08/19/2002
Decision Date
10/16/2002
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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