Greiner Bio-One Vacuette North America is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Greiner Bio-One Vacuette North America - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Greiner Bio-One Vacuette North America has 5 FDA 510(k) cleared medical devices. Based in Baldwin, US.
Historical record: 5 cleared submissions from 2001 to 2008. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Greiner Bio-One Vacuette North America Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Greiner Bio-One Vacuette North America
5 devices
Cleared
Apr 24, 2008
SAFETY INFUSION SET
General Hospital
85d
Cleared
Apr 15, 2005
VACUETTE EDTA K3 EVACUATED BLOOD COLLECTION TUBES
Chemistry
175d
Cleared
Dec 29, 2003
VACUETTE QUICKSHIELD SAFETY TUBE HOLDER
General Hospital
56d
Cleared
Jan 27, 2003
VACUETTE TRACE ELEMENTS TUBES
Chemistry
59d
Cleared
Jun 28, 2001
VACUETTE EVACUATED BLOOD COLLECTION TUBES
Chemistry
27d