K250779
- 510(k) number
- K250779
- Device name
- CS-Pro MED
- Applicant
- Curative Sound Therapeutics IN · US
- Product code
- PZL — Extracorporeal Shock Wave Device For Treatment Of Di
- Decision date
- 2025-07-02
- Date received
- 2025-03-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K250779.pdf
Official FDA record: K250779
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.