Greiner America, Inc.
Greiner America, Inc. appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 4, 1997.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K971220 | GREINER VACUETTE BLOOD COLLECTION TUBE | June 4, 1997 |
| K971236 | GREINER VACUETTE BLOOD COLLECTION TUBE | May 12, 1997 |
| K971239 | GREINER VACUETTE BLOOD COLLECTION TUBE | May 12, 1997 |
| K971221 | GREINER VACUETTE BLOOD COLLECTION TUBE | May 2, 1997 |
| K960860 | GREINER VACUETTE BLOOD COLLECTION TUBE E/EDTA K3 | September 5, 1996 |
| K960857 | GREINER VACUETTE BLOOD COLLECTION TUBE W/LITHIUM HEPARIN & GEL SEPARATOR | August 30, 1996 |
| K960858 | GREINER VACUTTE BLOOD COLLECTION TUBE W/ CLOT ACTIVATOR & GEL SEPARATOR | August 30, 1996 |