FDA 510(k) Applications Submitted by BostonSight
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K161461 | 05/26/2016 | BostonSight PD Prosthetic Device | BostonSight |
| K183175 | 11/16/2018 | BostonSight Scleral | BostonSight |
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