FDA 510(k) Applications Submitted by KONICA MINOLTA INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K133730 | 12/06/2013 | CO PILOT/REGIUS UNITEA | KONICA MINOLTA INC. |
| K142197 | 08/11/2014 | ULTRASOUND SYSTEM SONIMAGE HS1, LINEAR PROBE L18-4, CONVEX PROBE C5-2 | KONICA MINOLTA INC. |
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