K252704
- 510(k) number
- K252704
- Device name
- F Care RF System (00MEDRF4000US, 05RAFAELOPROBE, 05SPHERAPROBE, 06OUTPUTKAB, 06Pedal1St)
- Applicant
- F Care Systems USA, LLC FL · US
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2025-11-24
- Date received
- 2025-08-27
- 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: K252704.pdf
Official FDA record: K252704
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.