FDA 510(k) Application Details - K013988

Device Classification Name Filter, Conduction, Anesthetic

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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
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Regulation Number 868.5130

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Classification Product Code BSN
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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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