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FDA 510(k) Application Details - K130664
Device Classification Name
Filter, Bacterial, Breathing-Circuit
More FDA Info for this Device
510(K) Number
K130664
Device Name
Filter, Bacterial, Breathing-Circuit
Applicant
A-M SYSTEMS
24301 WOODSAGE DR.
BONITA SPRINGS, FL 34134 US
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Contact
PAUL DRYDEN
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Regulation Number
868.5260
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Classification Product Code
CAH
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More FDA Info for this Product Code
Date Received
03/12/2013
Decision Date
06/21/2013
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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