K-number	K210920
Device name	iBOT Personal Mobility Device (iBOT PMD)
Applicant	Mobius Mobility
Product code	IMK
Device class	Class II
Decision date	Jun 16, 2021
Decision	Substantially Equivalent
Regulation	890.3890

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Source

View the full FDA submission: accessdata.fda.gov

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iBOT Personal Mobility Device (iBOT PMD)

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