Biosite Incorporated · Class II · Cleared Jan 10, 2002
| K-number | K012745 |
| Device name | TRIAGE TOX DRUG SCREEN, CATALOG #94000 |
| Applicant | Biosite Incorporated |
| Product code | DKZ |
| Device class | Class II |
| Decision date | Jan 10, 2002 |
| Decision | Substantially Equivalent |
| Regulation | 862.3100 |
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