510(k) DEN160029 ยท QAI Powered Microneedle Device
SkinPen Precision System
| Applicant | Bellus Medical, LLC, Dallas TX, US |
| Decision | Unknown, Mar 1, 2018 |
| Received | Jul 5, 2016 |
| Type | Direct |
| FDA record | Open on fda.gov |
Recalls that name DEN160029
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.