FDA 510(k) Applications Submitted by Brian Smith
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K192138 | 08/08/2019 | Rejuvapen NXT | Refine USA LLC |
| K112334 | 08/12/2011 | VEIN-GOGH INSTRUMENT | REFINE USA, LLC |
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