Device details
FDA 510(k) registration fields
- K number
- K260100
- Device name
- MOSES Raydar™
- Country / region
- United States(US)
- Product code
- GEX
- Device class
- Class 2
- Regulation number
- 21 CFR 878.4810
- Date received
- 2026-01-13
- Decision date
- 2026-05-18
- Submission type
- Traditional
