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FDA 510(k)

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

K-Number: K241751 · 2024-07-15

ApplicantPositrigo AG
Decision Date2024-07-15
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NeuroLF (Basic); NeuroLF (Pro); NeuroLF (Advanced); NeuroLF Seat is a medical device manufactured by Positrigo AG. It received FDA 510(k) clearance on 2024-07-15 under approval number K241751. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NeuroLF (Basic); NeuroLF (Pro); NeuroLF (Advanced); NeuroLF Seat?

NeuroLF (Basic); NeuroLF (Pro); NeuroLF (Advanced); NeuroLF Seat is a medical device that received FDA 510(k) clearance on 2024-07-15. It is manufactured by Positrigo AG. The 510(k) number is K241751.

When was NeuroLF (Basic); NeuroLF (Pro); NeuroLF (Advanced); NeuroLF Seat approved by the FDA?

NeuroLF (Basic); NeuroLF (Pro); NeuroLF (Advanced); NeuroLF Seat received FDA 510(k) clearance on 2024-07-15, under approval number K241751.

What company makes NeuroLF (Basic); NeuroLF (Pro); NeuroLF (Advanced); NeuroLF Seat?

NeuroLF (Basic); NeuroLF (Pro); NeuroLF (Advanced); NeuroLF Seat is manufactured by Positrigo AG.

What is the FDA product code for NeuroLF (Basic); NeuroLF (Pro); NeuroLF (Advanced); NeuroLF Seat?

The FDA product code for NeuroLF (Basic); NeuroLF (Pro); NeuroLF (Advanced); NeuroLF Seat is KPS.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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