Medical Device Manufacturer · US , Plano , TX

Vedi Corp. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2004

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Vedi Corp. Anesthesiology ✕

1 devices

1-1 of 1

Cleared Jan 30, 2004

VADI MANUAL RESUSCITATOR

Anesthesiology · 318d