Medical Device Manufacturer · US , Mccordsville , IN

Fuji Systems Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2005

Recent clearances: CELLO BALLOON GUIDE CATHETER (6F), 950 MM AND 1020 MM LENGTH, SILBRONCHO DOUBLE LUMEN TUBE

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

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

1 devices

1-1 of 1

Cleared Aug 17, 2005

SILBRONCHO DOUBLE LUMEN TUBE

Anesthesiology · 70d