FDA 510(k) Applications Submitted by Dunia Bram
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K220654 | 03/07/2022 | ANGIOGUARD XP Emboli Capture Guidewire, ANGIOGUARD RX Emboli Capture Guidewire | Cordis Corporation |
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