FDA 510(k)

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

K-Number: K241751 · 2024-07-15

Decision Date2024-07-15

Product CodeKPS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

NeuroLF (Basic); NeuroLF (Pro); NeuroLF (Advanced); NeuroLF Seat is the device name listed in this FDA 510(k) record. The listed applicant is Positrigo AG. It received FDA 510(k) clearance on 2024-07-15 under 510(k) 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. The listed applicant is Positrigo AG. The 510(k) number is K241751.

When did NeuroLF (Basic); NeuroLF (Pro); NeuroLF (Advanced); NeuroLF Seat receive FDA 510(k) clearance?

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

Who is the listed applicant for NeuroLF (Basic); NeuroLF (Pro); NeuroLF (Advanced); NeuroLF Seat?

The FDA 510(k) record lists Positrigo AG as the applicant. This does not by itself establish the device manufacturer.

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.

Related Devices (Code: KPS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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