510(k) K150172 ยท LRC Instrument, Ent Manual Surgical
ACCLARENT SE Inflation Device
| Applicant | Acclarent, Inc., Rmenlo Park CA, US |
| Decision | Substantially Equivalent, Apr 7, 2015 |
| Received | Jan 26, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K150172
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.