FDA 510(k) Application Details - K090777

Device Classification Name Tube, Tracheal (W/Wo Connector)

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510(K) Number K090777
Device Name Tube, Tracheal (W/Wo Connector)
Applicant EZC MEDICAL, LLC
16 A FUNSTON AVENUE
SAN FRANCISCO, CA 94129 US
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Contact PAVAN SETHI
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Regulation Number 868.5730

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Classification Product Code BTR
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Date Received 03/23/2009
Decision Date 08/04/2009
Decision SESE - SUBST EQUIV
Classification Advisory Committee AN - Anesthesiology
Review Advisory Committee AN - Anesthesiology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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