K233751
- 510(k) number
- K233751
- Device name
- Milieve (YPS-301BD)
- Applicant
- Soterix Medical, Inc. NJ · US
- Product code
- PCC — Stimulator, Nerve, Electrical, Transcutaneous, For M
- Decision date
- 2024-06-03
- Date received
- 2023-11-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K233751.pdf
Official FDA record: K233751
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.