FDA 510(k) Application Details - K760611

Device Classification Name Filter, Bacterial, Breathing-Circuit

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510(K) Number K760611
Device Name Filter, Bacterial, Breathing-Circuit
Applicant 3M COMPANY
8124 PACIFIC AVE.
WHITE CITY, OR US
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Regulation Number 868.5260

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Classification Product Code CAH
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Date Received 09/10/1976
Decision Date 09/21/1976
Decision SE - Substantially Equivalent
Classification Advisory Committee CV - Cardiovascular
Review Advisory Committee AN - Anesthesiology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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