510(k) DEN170086 ยท QBR Intranasal Electrostimulation Device For Dry Eye Symptoms
TrueTear Intranasal Tear Neurostimulator
| Applicant | Allergan, Irvine CA, US |
| Decision | Unknown, May 17, 2018 |
| Received | Oct 23, 2017 |
| Type | Direct |
| FDA record | Open on fda.gov |
Recalls that name DEN170086
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.