FDA 510(k) Application Details - K131707

Device Classification Name Ventilator, Non-Continuous (Respirator)

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510(K) Number K131707
Device Name Ventilator, Non-Continuous (Respirator)
Applicant 3B MEDICAL, INC
21301 HWY 27 N
Lake Wales, FL 33859 US
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Contact ALEX LUCIO
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Regulation Number 868.5905

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Classification Product Code BZD
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Date Received 06/11/2013
Decision Date 08/22/2013
Decision SESE - SUBST EQUIV
Classification Advisory Committee AN - Anesthesiology
Review Advisory Committee AN - Anesthesiology
Statement / Summary / Purged Status Summary
Type Special
Reviewed By Third Party N
Expedited Review



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