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FDA 510(k) Application Details - K951927
Device Classification Name
Catheter, Conduction, Anesthetic
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510(K) Number
K951927
Device Name
Catheter, Conduction, Anesthetic
Applicant
CSEN LTD.
P.O. BOX 27476
JERUSALEM 91273
ISRAEL IL
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Contact
JOSEPH ELDOR
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Regulation Number
868.5120
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Classification Product Code
BSO
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Date Received
04/24/1995
Decision Date
05/30/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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