NQ TMS for MDD (NQv1-MU-01)
K-Number: K232688 · 2023-12-29
Device Summary
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. The listed applicant is Neuroqore, Inc.. The 510(k) number is K232688.
When did NQ TMS for MDD (NQv1-MU-01) receive FDA 510(k) clearance?
NQ TMS for MDD (NQv1-MU-01) received FDA 510(k) clearance on 2023-12-29, under 510(k) number K232688.
Who is the listed applicant for NQ TMS for MDD (NQv1-MU-01)?
The FDA 510(k) record lists Neuroqore, Inc. as the applicant. This does not by itself establish the device manufacturer.
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.
Related Devices (Code: OBP)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.