K-number	K232930
Device name	VERVE
Applicant	Oculomotor Technologies
Product code	SBN
Device class	Class I
Decision date	Jun 13, 2024
Decision	Substantially Equivalent
Regulation	886.1290

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Source

View the full FDA submission: accessdata.fda.gov

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VERVE

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