Class Class II

NeuroLF (Basic); NeuroLF (Pro); NeuroLF (Advanced); NeuroLF Seat (K241751)

K241751 2024-07-15 Abbreviated
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Description

NeuroLF (Basic); NeuroLF (Pro); NeuroLF (Advanced); NeuroLF Seat by Positrigo AG — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241751
Clearance Date2024-07-15
Clearance TypeAbbreviated
Product CodeKPS
Regulation Number892.1200

Categories

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