FDA 510(k) Applications Submitted by James Childs
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K192331 | 08/27/2019 | LaseMD LEO Laser System | Lutronic Global |
| K183566 | 12/21/2018 | CLARITY II Laser System | Lutronic Corporation |
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