FDA 510(k) Applications Submitted by ALLIQUA BIOMEDICAL, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K162721 | 09/29/2016 | Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator | ALLIQUA BIOMEDICAL, INC. |
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