K250275
- 510(k) number
- K250275
- Device name
- PrecisePath Radiofrequency Puncture Generator and PrecisePath Footswitch
- Applicant
- Baylis Medical Technologies, Inc. CA
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2025-10-28
- Date received
- 2025-01-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K250275.pdf
Official FDA record: K250275
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.