FDA 510(k) Applications Submitted by Peter Bather
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K230191 | 01/24/2023 | AriseÖ UHP Dilatation Catheter | Creagh Medical Ltd |
| K231828 | 06/21/2023 | PounceÖ Sheath | Surmodics, Inc. |
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