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FDA 510(k) Application Details - K980884
Device Classification Name
Vaporizer, Anesthesia, Non-Heated
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510(K) Number
K980884
Device Name
Vaporizer, Anesthesia, Non-Heated
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
16 ELECTRONICS AVE.
DANVERS, MA 01923 US
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DAVID SIMARD
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Regulation Number
868.5880
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Classification Product Code
CAD
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Date Received
03/09/1998
Decision Date
08/19/1998
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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