FDA 510(k) Applications Submitted by Osprey Medical Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K190102 | 01/22/2019 | DyeVertÖ Plus Contrast Reduction System, DyeTectÖ Contrast Monitoring System, DyeVertÖ Plus EZ Contrast Reduction System | Osprey Medical Inc. |
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