FDA 510(k) Applications Submitted by Becton, Dickinson and Company (Bard Access Systems, Inc.)
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K240359 | 02/06/2024 | PowerGlide ProÖ Midline Catheter | Becton, Dickinson and Company (Bard Access Systems, Inc.) |
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