FDA 510(k) Applications Submitted by Cardio Flow, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K231538 | 05/30/2023 | FreedomFlow Orbital Circumferential Atherectomy System | Cardio Flow, Inc. |
| K213834 | 12/09/2021 | Cardio Flow Peripheral Guide Wire | Cardio Flow, Inc. |
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