FDA 510(k) Applications Submitted by UroViu Corporation
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K232837 | 09/14/2023 | Uro-G HD Flexible Cystoscope | UroViu Corporation |
| K171500 | 05/23/2017 | Uro-V Cystoscope | UroViu Corporation |
| K202921 | 09/29/2020 | Uro-G Cystoscope | UroViu Corporation |
| K243196 | 10/01/2024 | Uro-G HD Cystoscope (1520) | UroViu Corporation |
| K182876 | 10/12/2018 | Uro-N Cystoscope | UroViu Corporation |
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