K-number	K210265
Device name	VS3 Iridium Sytem
Applicant	Visionsense, Ltd.
Product code	OWN
Device class	Class II
Decision date	Nov 22, 2021
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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VS3 Iridium Sytem

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