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FDA 510(k) Application Details - K050066
Device Classification Name
Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
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510(K) Number
K050066
Device Name
Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
Applicant
MARQUEST MEDICAL PRODUCTS, INC.
11039 EAST LANSING CIR.
ENGLEWOOD, CO 80112 US
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Contact
THOMAS W DIELMANN
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Regulation Number
868.1400
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Classification Product Code
CCK
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More FDA Info for this Product Code
Date Received
01/12/2005
Decision Date
03/01/2005
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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