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FDA 510(k) Application Details - K143164
Device Classification Name
Catheter, Conduction, Anesthetic
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510(K) Number
K143164
Device Name
Catheter, Conduction, Anesthetic
Applicant
KIMBERLY-CLARK CORPORATION
43 DISCOVERY, SUITE 100
IRVINE, CA 92618 US
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Contact
MARIA E WAGNER
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Regulation Number
868.5120
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Classification Product Code
BSO
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More FDA Info for this Product Code
Date Received
11/03/2014
Decision Date
12/02/2014
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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