FDA 510(k) Applications Submitted by Cross Vascular Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K232809 | 09/12/2023 | Cross Vascular RF Generator and Footswitch (optional accessory) | Cross Vascular Inc. |
| K232852 | 09/14/2023 | Cross Vascular RF Transseptal Needle, Cross Vascular Connection Cable | Cross Vascular Inc. |
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