510(k) K193589 ยท QBR Intranasal Electrostimulation Device For Dry Eye Symptoms
TrueTear Intranasal Tear Neurostimulator
| Applicant | Allergan, Irvine CA, US |
| Decision | Substantially Equivalent, Aug 31, 2020 |
| Received | Dec 23, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K193589
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.