Medical Device Manufacturer · GB , Runcorn

Shandon Diagnostics Limited - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2025

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Shandon Diagnostics Limited Pathology ✕

1 devices

1-1 of 1

Cleared Feb 28, 2025

E1000 Dx Digital Pathology Solution

Pathology · 259d