FDA 510(k) Application Details - K052954

Device Classification Name Anesthesia Conduction Kit

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510(K) Number K052954
Device Name Anesthesia Conduction Kit
Applicant LIFE-TECH, INC.
4235 GREENBRIAR DR.
STAFFORD, TX 77477-3995 US
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Contact JEFF KASOFF
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Regulation Number 868.5140

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Classification Product Code CAZ
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Date Received 10/20/2005
Decision Date 02/15/2006
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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