Medical Device Manufacturer · US , Keene , NH

Concord/Portex - FDA 510(k) Cleared Devices

23 submissions · 20 cleared · Since 1989

23

Total

20

Cleared

0

Denied

FDA 510(k) Regulatory Record - Concord/Portex Obstetrics & Gynecology ✕

1 devices

1-1 of 1

Cleared Jan 12, 1990

AMNIOTIC FLUID SAMPLER (AMNIOCENTESIS TRAY)

Obstetrics & Gynecology · 88d