FDA 510(k) Application Details - K092451

Device Classification Name Filter, Bacterial, Breathing-Circuit

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510(K) Number K092451
Device Name Filter, Bacterial, Breathing-Circuit
Applicant INTERSURGICAL, INC.
417 ELECTRONICS PKWY.
LIVERPOOL, NY 13088 US
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Contact MICHAEL ZALEWSKI
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Regulation Number 868.5260

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Classification Product Code CAH
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Date Received 08/10/2009
Decision Date 10/29/2010
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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