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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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