Medical Device Manufacturer · US , Palo Alto , CA

Tidepool Project - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2023

Total

Cleared

Denied

Tidepool Project has 1 FDA 510(k) cleared medical devices. Based in Palo Alto, US.

Last cleared in 2023. Active since 2023. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Tidepool Project Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Tidepool Project

1 devices

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