FDA 510(k) Applications Submitted by KONICA MINOLTA TECHNOPRODUCT CO., LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K082347 | 08/15/2008 | DIGITAL RADIOGRAPHY, FLEXDR C30 | KONICA MINOLTA TECHNOPRODUCT CO., LTD. |
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