FDA 510(k)

NeuroTrigger Basic (NTB)

K-Number: K223027 · 2023-10-10

Decision Date2023-10-10

Product CodeIPF

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

NeuroTrigger Basic (NTB) is the device name listed in this FDA 510(k) record. The listed applicant is Neurotrigger. It received FDA 510(k) clearance on 2023-10-10 under 510(k) number K223027. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NeuroTrigger Basic (NTB)?

NeuroTrigger Basic (NTB) is a medical device that received FDA 510(k) clearance on 2023-10-10. The listed applicant is Neurotrigger. The 510(k) number is K223027.

When did NeuroTrigger Basic (NTB) receive FDA 510(k) clearance?

NeuroTrigger Basic (NTB) received FDA 510(k) clearance on 2023-10-10, under 510(k) number K223027.

Who is the listed applicant for NeuroTrigger Basic (NTB)?

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

What is the FDA product code for NeuroTrigger Basic (NTB)?

The FDA product code for NeuroTrigger Basic (NTB) is IPF.

Related Devices (Code: IPF)

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.

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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.