Liquidmetal Technologies Inc (LQMT)

[Researchfyi]

Regarding the FDA pre market 510K by MOVE…

This is what I found. It is from a filed 8K 11-15-23

“Following the submission of its 510(k) application to the FDA for the Evie Ring’s pulse oximeter in July 2023, Movano Health has since received a letter from the FDA requesting additional information, which was in line with the Company’s expectations. The Company has been in communication with the agency and plans to submit its formal reply letter to the FDA in Q1 2024. If clearance is received, it has the potential to unlock a significant enterprise opportunity with partners across healthcare”

This “medical device company “ I believe from the documents I reviewed started the intended 510K approval process in 2021.

Good luck to all in LQMT.
Wish TC luck.