Medical Device Manufacturer · GB , Oxon Ox8 1ja England

Oakfield Instruments, Ltd. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1989

Recent clearances: FLEXILOG LS, FLEXILOG 3000, FLEXILOG LS 13921

View 8 510(k) Devices ↓

8

Total

8

Cleared

0

Denied

FDA 510(k) Regulatory Record - Oakfield Instruments, Ltd. Toxicology ✕

1 devices

1-1 of 1

Cleared Oct 17, 1989

Toxicology · 77d