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FDA 510(k) Application Details - K013988
Device Classification Name
Filter, Conduction, Anesthetic
More FDA Info for this Device
510(K) Number
K013988
Device Name
Filter, Conduction, Anesthetic
Applicant
MILLIPORE CORP.
80 ASHBY RD.
BEDFORD, MA 01730 US
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Contact
THOMAS BORROWS
Other 510(k) Applications for this Contact
Regulation Number
868.5130
More FDA Info for this Regulation Number
Classification Product Code
BSN
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/04/2001
Decision Date
04/04/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Statement
Type
Special
Reviewed By Third Party
N
Expedited Review
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