Medical Device Manufacturer · US , New York , NY

N-Dia, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2004

Recent clearances: AMNISURE FETAL MEMBRANES RUPTURE TEST MODEL FMRT1

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - N-Dia, Inc. Chemistry ✕

1 devices

1-1 of 1

Cleared Feb 02, 2004

AMNISURE FETAL MEMBRANES RUPTURE TEST MODEL FMRT1

Chemistry · 322d