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FDA 510(k)

NQ TMS for MDD (NQv1-MU-01)

K-Number: K232688 · 2023-12-29

ApplicantNeuroqore, Inc.
Decision Date2023-12-29
Product CodeOBP
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NQ TMS for MDD (NQv1-MU-01) is a medical device manufactured by Neuroqore, Inc.. It received FDA 510(k) clearance on 2023-12-29 under approval number K232688. The device is classified under product code OBP. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NQ TMS for MDD (NQv1-MU-01)?

NQ TMS for MDD (NQv1-MU-01) is a medical device that received FDA 510(k) clearance on 2023-12-29. It is manufactured by Neuroqore, Inc.. The 510(k) number is K232688.

When was NQ TMS for MDD (NQv1-MU-01) approved by the FDA?

NQ TMS for MDD (NQv1-MU-01) received FDA 510(k) clearance on 2023-12-29, under approval number K232688.

What company makes NQ TMS for MDD (NQv1-MU-01)?

NQ TMS for MDD (NQv1-MU-01) is manufactured by Neuroqore, Inc..

What is the FDA product code for NQ TMS for MDD (NQv1-MU-01)?

The FDA product code for NQ TMS for MDD (NQv1-MU-01) is OBP.

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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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