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FDA 510(k) Application Details - K021920
Device Classification Name
Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)
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510(K) Number
K021920
Device Name
Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)
Applicant
COOK, INC.
P.O. BOX 489
BLOOMINGTON, IN 47402-0489 US
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APRIL LAVENDER
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Regulation Number
868.5740
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Classification Product Code
CBI
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More FDA Info for this Product Code
Date Received
06/11/2002
Decision Date
08/14/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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