510(k) K190525 ยท LRC Instrument, Ent Manual Surgical
RELIEVA ULTIRRA Sinus Balloon Catheter
| Applicant | Acclarent, Inc., Irvin CA, US |
| Decision | Substantially Equivalent, May 3, 2019 |
| Received | Mar 4, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190525
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.