FDA 510(k) Applications Submitted by FaceHeart Corp.

FDA 510(k) Number Submission Date Device Name Applicant
K243966 12/23/2024 FaceHeart Vitals Software Development Kit (FH vitals SDK-RR) FaceHeart Corp.
K223622 12/05/2022 FaceHeart Vitals Software Development Kit (FH vitals SDK) FaceHeart Corp.


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