K260287
- 510(k) number
- K260287
- Device name
- SP Electrocautery Device (SP20)
- Applicant
- Single Pass, Inc. CA · US
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2026-02-24
- Date received
- 2026-01-29
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K260287.pdf
Official FDA record: K260287
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.