K-number	K210947
Device name	Navident
Applicant	Claronav, Inc.
Product code	PLV
Device class	Class II
Decision date	Jun 27, 2022
Decision	Substantially Equivalent
Regulation	872.4120

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Source

View the full FDA submission: accessdata.fda.gov

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Navident

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