Medical Device Manufacturer · BE , Leuven

Terumo Europe N.V. - FDA 510(k) Cleared Devices

28 submissions · 28 cleared · Since 1999

28

Total

28

Cleared

0

Denied

28 devices

26-28 of 28

Cleared May 28, 2004

VENOJECT LUER ADAPTER

Chemistry · 7d

Cleared Aug 14, 2000

General Hospital · 84d

Cleared Jun 14, 1999

K-PACK II (HYPODERMIC NEEDLE) 23G X 1, MODEL KN-2325RB, K-PACK II NEEDLE...

General Hospital · 173d