FDA 510(k) Applications Submitted by Imaxeon Pty Ltd
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K241849 | 06/27/2024 | MEDRAD Centargo CT Injection System; MEDRAD Centargo Day Set; MEDRAD Centargo Patient Line; MEDRAD Centargo Replacement Spike; MEDRAD ISI2 Module (ISI2) | Imaxeon Pty Ltd |
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