K232688
- 510(k) number
- K232688
- Device name
- NQ TMS for MDD (NQv1-MU-01)
- Applicant
- Neuroqore, Inc. CA · US
- Product code
- OBP — Transcranial Magnetic Stimulator
- Decision date
- 2023-12-29
- Date received
- 2023-09-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K232688.pdf
Official FDA record: K232688
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.