Medical Device Manufacturer · US , Santee , CA

Pathway, LLC - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2016

Total

Cleared

Denied

Pathway, LLC has 3 FDA 510(k) cleared medical devices. Based in Santee, US.

Historical record: 3 cleared submissions from 2016 to 2020. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) cleared devices by Pathway, LLC

3 devices

1-3 of 3