FDA 510(k) Application Details - K862786

Device Classification Name Filter, Bacterial, Breathing-Circuit

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510(K) Number K862786
Device Name Filter, Bacterial, Breathing-Circuit
Applicant MEDIPART JERRY ALEXANDER
607 SPRING BEACH RD.
CARY, IL US
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Contact JERRY ALEXANDER
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Regulation Number 868.5260

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Classification Product Code CAH
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Date Received 07/23/1986
Decision Date 08/01/1986
Decision SE - Substantially Equivalent
Classification Advisory Committee AN - Anesthesiology
Review Advisory Committee AN - Anesthesiology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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