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FDA 510(k) Application Details - K023233
Device Classification Name
Catheter, Conduction, Anesthetic
More FDA Info for this Device
510(K) Number
K023233
Device Name
Catheter, Conduction, Anesthetic
Applicant
EBI, L.P.
399 JEFFERSON ROAD
PARSIPPANY, NJ 07054 US
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Contact
JON CAPAROTTA
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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
09/27/2002
Decision Date
12/13/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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