K-number	K223622
Device name	FaceHeart Vitals Software Development Kit (FH vitals SDK)
Applicant	Faceheart Corp.
Product code	QME
Device class	Class II
Decision date	Sep 1, 2023
Decision	Substantially Equivalent
Regulation	870.2785

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Source

View the full FDA submission: accessdata.fda.gov

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FaceHeart Vitals Software Development Kit (FH vitals SDK)

Everything you need for a 510(k) submission. Nothing you don't.