Digital Color Doppler Ultrasound System (Marvo 95/Marvo 95 Elite/Marvo 90/Marvo 90 CV/Marvo 90 Pro/Marvo 90 Exp/Marvo 90 Elite/Marvo Expert/Marvo 85/Marvo 85 Pro/Marvo 85 Exp/Marvo 85 Elite/Marvo Senior/Marvo 75 Elite/Marvo 75i/Fenix 95/Fenix 95 Elite/Fenix 90/Fenix 90 Elite/Fenix Expert/Fenix 85/Fenix 85 Elite/Fenix Senior/Fenix 75 Elite/Fenix 75i/Endo 80/Endo 90)
K254027 is the FDA 510(k) clearance record for Digital Color Doppler Ultrasound System (Marvo 95/Marvo 95 Elite/Marvo 90/Marvo 90 CV/Marvo 90 Pro/Marvo 90 Exp/Marvo 90 Elite/Marvo Expert/Marvo 85/Marvo 85 Pro/Marvo 85 Exp/Marvo 85 Elite/Marvo Senior/Marvo 75 Elite/Marvo 75i/Fenix 95/Fenix 95 Elite/Fenix 90/Fenix 90 Elite/Fenix Expert/Fenix 85/Fenix 85 Elite/Fenix Senior/Fenix 75 Elite/Fenix 75i/Endo 80/Endo 90), a class II device, cleared for Sonoscape Medical Corp. on under FDA product code IYN (System, Imaging, Pulsed Doppler, Ultrasonic). As of , FDA records show no recalls naming K254027.
Clearance record
Clearances, product code IYN
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 6 |
| December 2025 | 6 |
| January 2026 | 4 |
| February 2026 | 1 |
| March 2026 | 6 |
| April 2026 | 3 |
| May 2026 | 11 |
| June 2026 | 3 |
| July 2026 | 6 |
| August 2026 | 3 |
| September 2026 | 3 |
| October 2026 | 0 |
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