Syncor Pharmaceuticals, Inc. · Class II · Cleared Dec 23, 1999
| K-number | K992008 |
| Device name | PHARMASEED, MODEL BT-125-1 |
| Applicant | Syncor Pharmaceuticals, Inc. |
| Product code | KXK |
| Device class | Class II |
| Decision date | Dec 23, 1999 |
| Decision | Substantially Equivalent |
| Regulation | 892.5730 |
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