FDA 510(k) Applications Submitted by Charles Reisman
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K161509 | 06/01/2016 | 3D OCT-1 Maestro | Topcon Corporation |
| K173119 | 09/29/2017 | DRI OCT Triton | Topcon Corporation |
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