K-number	K241751
Device name	NeuroLF (Basic); NeuroLF (Pro); NeuroLF (Advanced); NeuroLF Seat
Applicant	Positrigo AG
Product code	KPS
Device class	Class II
Decision date	Jul 15, 2024
Decision	Substantially Equivalent
Regulation	892.1200

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Source

View the full FDA submission: accessdata.fda.gov

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NeuroLF (Basic); NeuroLF (Pro); NeuroLF (Advanced); NeuroLF Seat

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