510(k) K183090 ยท QGK Balloon, Nasal Airway
Relieva Tract Balloon Dilation System
| Applicant | Acclarent, Inc., Irvin CA, US |
| Decision | Substantially Equivalent, Apr 19, 2019 |
| Received | Nov 6, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183090
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.