Medical Device Manufacturer · IT , Campli (Teramo)

Pentaferte, S.R.L. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2001

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Pentaferte, S.R.L. General Hospital ✕

1 devices

1-1 of 1

Cleared Jan 11, 2001

PENTAFERTE SINGLE USE SYRINGES, MODEL SIZE=VARIOUS SIZES

General Hospital · 160d