K260100
- 510(k) number
- K260100
- Device name
- MOSES Raydar
- Applicant
- Boston Scientific Corporation MA · US
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2026-05-18
- Date received
- 2026-01-13
- 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: K260100.pdf
Official FDA record: K260100
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.