FDA 510(k) Applications Submitted by Tanya Shalem
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K230370 | 02/10/2023 | SpotLight/SpotLight Duo (with DLIR option) | Arineta Ltd. |
| K213465 | 10/28/2021 | CardioGraphe | Arineta Ltd. |
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