510(k) K052198 ยท LRC Instrument, Ent Manual Surgical
RELIEVA SINUS BALLOON INFLATION DEVICE
| Applicant | Acclarent, Inc., Rmenlo Park CA, US |
| Decision | Substantially Equivalent, Aug 31, 2005 |
| Received | Aug 12, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052198
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.