K-number	K240794
Device name	Frontier X Plus
Applicant	Fourth Frontier Technologies Pvt, Ltd.
Product code	MLO
Device class	Class II
Decision date	Nov 8, 2024
Decision	Substantially Equivalent
Regulation	870.2800

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Source

View the full FDA submission: accessdata.fda.gov

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Frontier X Plus

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