Medical Device Manufacturer · ES , Barcelona

Leventon, S.A. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1985

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - Leventon, S.A. General Hospital ✕

3 devices

1-3 of 3

Cleared Apr 07, 2004

General Hospital · 14d

Cleared Sep 08, 1995

DOSI-FLOW, MODELS 20 & 30

General Hospital · 81d

Cleared Apr 29, 1985

General Hospital · 46d