Greiner America, Inc. · Class II · Cleared May 12, 1997
| K-number | K971236 |
| Device name | GREINER VACUETTE BLOOD COLLECTION TUBE |
| Applicant | Greiner America, Inc. |
| Product code | JKA |
| Device class | Class II |
| Decision date | May 12, 1997 |
| 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