| K-number | K041578 |
| Device name | QUICKSCREEN, MODELS 9177X AND 9178X |
| Applicant | Phamatech |
| Product code | LCM |
| Device class | Class U |
| Decision date | Sep 10, 2004 |
| Decision | Substantially Equivalent |
| Regulation | — |
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