FDA 510(k) Application Details - K120518

Device Classification Name Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase

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510(K) Number K120518
Device Name Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
Applicant CAREFUSION
1500 WAUKEGAN ROAD
WAUKEGAN, IL 60085 US
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Contact ERIKA FERNANDEZ
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Regulation Number 868.1400

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Classification Product Code CCK
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Date Received 02/21/2012
Decision Date 05/04/2012
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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