Medicatech USA
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K230918 | MasterX 800 Series | MQB | 2023-09-01 | View |
| 510(k) | K190601 | MasteRad MX30 | KPR | 2019-04-25 | View |
| 510(k) | K130377 | KRYSTALRAD NEW SERIESDIGITAL RADIOGRAPHIC PORTABLE RETROFIT SYSTEM | MQB | 2013-05-17 | View |
| 510(k) | K112132 | KRYSTALRAD 660 DIGITAL RADIOGRAPHIC PORTABLE RETROFIT SYSTEM | MQB | 2011-11-18 | View |
| 510(k) | K102284 | KRYSTALRAD 560 (FLAATZ 560) | KPR | 2011-01-03 | View |
| 510(k) | K102285 | KRYSTALRAD (ATAL8) | KPR | 2011-01-03 | View |
| 510(k) | K082798 | DIGITAL DIAGNOSTIC X-RAY SYSTEM, MODELS MAK 1500, MAK 2000 AND MAK 3000 | KPR | 2008-10-28 | View |
| 510(k) | K080582 | MEDICATECH, MODEL DDR MAK-800, DDT MAK-1000 FS, DDR MAK-1100 FA | KPR | 2008-05-15 | View |
No matching devices.
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