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FDA 510(k) Application Details - K963717
Device Classification Name
Filter, Conduction, Anesthetic
More FDA Info for this Device
510(K) Number
K963717
Device Name
Filter, Conduction, Anesthetic
Applicant
MILLIPORE CORP.
80 ASHBY RD.
P.O. BOX 9125
BEDFORD, MA 01730 US
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Contact
THOMAS G BORROWS
Other 510(k) Applications for this Contact
Regulation Number
868.5130
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Classification Product Code
BSN
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More FDA Info for this Product Code
Date Received
09/16/1996
Decision Date
06/10/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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