Medical Device Manufacturer · GB , Cambridge

Cytocell, Ltd. - FDA 510(k) Cleared Devices

1 submissions · 0 cleared · Since 2018

1

Total

0

Cleared

1

Denied

FDA 510(k) Regulatory Record - Cytocell, Ltd. Medical Genetics ✕

1 devices

1-1 of 1

Not Cleared Dec 21, 2018

MLL (KMT2A) Breakapart FISH Probe Kit

DEN170070 · QDI

Medical Genetics · 448d