Medical Device Manufacturer · US , Salt Lake City , UT

Maxtec, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2004

Total

Cleared

Denied

Maxtec, Inc. has 4 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.

Historical record: 4 cleared submissions from 2004 to 2014. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Maxtec, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Maxtec, Inc.

4 devices

1-4 of 4