FDA 510(k) Applications Submitted by MAXTEC, LLC

FDA 510(k) Number Submission Date Device Name Applicant
K161718 06/22/2016 MaxBlend 2, MaxBlend Lite Maxtec, LLC
K153659 12/21/2015 MaxO2ME MAXTEC, LLC
K221734 06/15/2022 Maxtec MaxO2 ME+p Maxtec, LLC
K112402 08/22/2011 ULTRAMAXO2 OXYGEN ANALYER MAXTEC, LLC
K182362 08/30/2018 MaxCap Ped and MaxCap Neo Maxtec, LLC


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