FDA 510(k) Applications Submitted by KONICA CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K992586 | 08/02/1999 | KONICA LASER IMAGER, DRYPRO MODEL 722 | KONICA CORP. |
| K990359 | 02/05/1999 | KONICA DIRECT DIGITIZER, MODEL DD-341 | KONICA CORP. |
| K980873 | 03/06/1998 | KONICA DIRECT DIGITIZER REGIUS MODEL 330 | KONICA CORP. |
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