Medical Device Manufacturer · US , New York , NY

Paige.Ai - FDA 510(k) Cleared Devices

1 submissions · 0 cleared · Since 2021

1

Total

0

Cleared

1

Denied

Paige.Ai has 0 FDA 510(k) cleared medical devices. Based in New York, US.

Active since 2021. Primary specialty: Pathology.

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

FDA 510(k) cleared devices by Paige.Ai

1 devices

1-1 of 1

Not Cleared Sep 21, 2021

DEN200080 · QPN

Pathology · 264d