Greiner America, Inc. · Class II · Cleared Aug 30, 1996
| K-number | K960858 |
| Device name | GREINER VACUTTE BLOOD COLLECTION TUBE W/ CLOT ACTIVATOR & GEL SEPARATOR |
| Applicant | Greiner America, Inc. |
| Product code | JKA |
| Device class | Class II |
| Decision date | Aug 30, 1996 |
| Decision | Substantially Equivalent |
| Regulation | 862.1675 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov