# K232688: NQ TMS for MDD (NQv1-MU-01)

- Pathway: 510(k) (Traditional)
- Applicant: Neuroqore, Inc.
- Decided: Dec 29, 2023 after 119 days
- Product code: OBP (Transcranial Magnetic Stimulator)
- Device class: 2
- Regulation: 21 CFR 882.5805
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to DEN070003 (2008). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K171481: MagVita TMS Therapy System, Tonica Elektronik A/S (2017) Summary page 5.
- K150641: MagVita TMS Therapy System, Tonica Elektronik A/S (2015) Summary page 5.

## Indications for use
The NQ TMS for MDD is indicated for the treatment of Major Depressive Disorder in adult patients who have failed to receive satisfactory improvement from prior antidepressant medication in the current episode.

Source page: https://510kreport.com/device/K232688
Methodology: https://510kreport.com/methodology