510(k) K120280 ยท LRC Instrument, Ent Manual Surgical
RELIEVA SEEKER BALLOON SINUPLASTY SYSTEM
| Applicant | Acclarent, Inc., Menlo Park CA, US |
| Decision | Substantially Equivalent, Nov 5, 2012 |
| Received | Jan 30, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120280
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.