Company ยท US
Greiner Bio-One Vacuette North America
FDA 510(k) clearances and medical device recalls filed under this name, 2001 to 2008. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Apr 24, 2008 | K080235 | SAFETY INFUSION SET Greiner Bio-One Vacuette North America | FMI |
| Apr 15, 2005 | K042927 | VACUETTE EDTA K3 EVACUATED BLOOD COLLECTION TUBES Greiner Bio-One Vacuette North America | PJE |
| Dec 29, 2003 | K033478 | VACUETTE QUICKSHIELD SAFETY TUBE HOLDER Greiner Bio-One Vacuette North America | FMI |
| Jan 27, 2003 | K023971 | VACUETTE TRACE ELEMENTS TUBES Greiner Bio-One Vacuette North America | JKA |
| Jun 28, 2001 | K011699 | VACUETTE EVACUATED BLOOD COLLECTION TUBES Greiner Bio-One Vacuette North America | JKA |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||