K241085
- 510(k) number
- K241085
- Device name
- Valleylab FT10 Energy Platform Software Version 5.0 (VLFT10GEN VLFT10FXGEN VLFT10LSGEN)
- Applicant
- Covidien, LLC CO · US
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2024-07-12
- Date received
- 2024-04-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 1.4 MB · U.S. public domain
Also available from FDA: K241085.pdf
Official FDA record: K241085
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.