Konica Corp.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K992586 | KONICA LASER IMAGER, DRYPRO MODEL 722 | LMC | 1999-10-29 | View |
| 510(k) | K990359 | KONICA DIRECT DIGITIZER, MODEL DD-341 | MQB | 1999-08-17 | View |
| 510(k) | K980873 | KONICA DIRECT DIGITIZER REGIUS MODEL 330 | LMA | 1998-06-19 | View |
| 510(k) | K920769 | KONICA LI 10 AND 10A LASER IMAGER | LMC | 1992-05-06 | View |
| 510(k) | K920558 | KONICA DIRECT DIGITIZER KD-1000 | KPR | 1992-03-06 | View |
No matching devices.
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