Medicatech USA · Class II · Cleared Feb 6, 2015
| K-number | K143257 |
| Device name | KrystalRad 11000 and KrystalRad 3000 Digital Stationary Radiographic System |
| Applicant | Medicatech USA |
| Product code | KPR |
| Device class | Class II |
| Decision date | Feb 6, 2015 |
| 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