FDA 510(k) Applications Submitted by Visionsense Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K150018 | 01/05/2015 | VS3-IR-MMS System | Visionsense Ltd. |
| K171208 | 04/25/2017 | Trans-anal Introducer | Visionsense Ltd. |
| K223020 | 09/29/2022 | VS3-Iridium System (VS3-IR) | Visionsense Ltd. |
| K210265 | 02/01/2021 | VS3 Iridium Sytem | Visionsense Ltd. |
| K141002 | 04/18/2014 | VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM | Visionsense Ltd. |
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