FDA 510(k) Applications Submitted by Christine Thomas
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K081021 | 04/10/2008 | KINETIX GUIDEWIRE, PLUS GUIDEWIRE | BOSTON SCIENTIFIC CORP. |
| K241693 | 06/12/2024 | FemChec Controlled Saline-Air Device (FCD-250) | Femasys Inc. |
| K231730 | 06/13/2023 | FemaSeed Intratubal Insemination | Femasys Inc. |
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