FDA 510(k) Applications Submitted by FEI GAO
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K121466 | 05/17/2012 | GUIDEMIA | GUIDEMIA TECHNOLOGIES, LLC |
| K162850 | 10/11/2016 | GuideMia Ortho+ | GUIDEMIA TECHNOLOGIES, LLC |
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