Medicatech USA · Class II · Cleared May 15, 2008
| K-number | K080582 |
| Device name | MEDICATECH, MODEL DDR MAK-800, DDT MAK-1000 FS, DDR MAK-1100 FA |
| Applicant | Medicatech USA |
| Product code | KPR |
| Device class | Class II |
| Decision date | May 15, 2008 |
| Decision | Substantially Equivalent |
| Regulation | 892.1680 |
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