FDA 510(k) Applications Submitted by Kamrie Sarnosky
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K230742 | 03/17/2023 | ACCLARENT AERA Eustachian Tube Dilation System | Acclarent, Inc. |
| K231862 | 06/23/2023 | TruDi« Navigation System V3 (FG-2000-00) | Acclarent, Inc. |
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