FDA 510(k) Applications Submitted by BrightWater Medical
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K161277 | 05/06/2016 | ConvertX Nephroureteral Stent System | BRIGHTWATER MEDICAL |
| K181669 | 06/25/2018 | ConvertX Biliary Stent System | BrightWater Medical |
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