Maxtec, LLC - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Maxtec, LLC has 6 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Last cleared in 2023. Active since 2011. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Maxtec, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Maxtec, LLC
6 devices
Cleared
Dec 04, 2023
Maxtec MaxBlend2+p
Anesthesiology
159d
Cleared
Apr 01, 2023
Maxtec MaxO2 ME+p
Anesthesiology
290d
Cleared
May 23, 2019
MaxCap Ped and MaxCap Neo
Anesthesiology
266d
Cleared
Oct 27, 2016
MaxBlend 2, MaxBlend Lite
Anesthesiology
127d
Cleared
Jun 10, 2016
MaxO2ME
Anesthesiology
172d
Cleared
Dec 14, 2011
ULTRAMAXO2 OXYGEN ANALYER
Anesthesiology
114d