FDA 510(k) Applications Submitted by Ultromics Limited
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K222463 | 08/15/2022 | EchoGo Heart Failure | Ultromics Limited |
| K213275 | 09/30/2021 | EchoGo Core (2.0) | Ultromics Limited |
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