Phamatech, Inc. · Class II · Cleared Feb 7, 2005
| K-number | K043051 |
| Device name | QUICKSCREEN OXYCODONE TEST, MODELS 9120, 9120T, 9120X AND 9121 |
| Applicant | Phamatech, Inc. |
| Product code | DJG |
| Device class | Class II |
| Decision date | Feb 7, 2005 |
| Decision | Substantially Equivalent |
| Regulation | 862.3650 |
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