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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