K-number	K240105
Device name	Navigator (FMNVG15); Navigator XL (FMNVX06)
Applicant	Forcemech International, LLC
Product code	ITI
Device class	Class II
Decision date	Aug 29, 2024
Decision	Substantially Equivalent
Regulation	890.3860

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Source

View the full FDA submission: accessdata.fda.gov

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Navigator (FMNVG15); Navigator XL (FMNVX06)

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