FDA 510(k) Applications Submitted by Acutus Medical Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K210685 | 03/08/2021 | AcQCross Qx Integrated Transseptal Dilator/Needle | Acutus Medical Inc. |
| K222209 | 07/25/2022 | AcQMap High Resolution Imaging and Mapping System | Acutus Medical Inc. |
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