510(k) K131709 ยท LRC Instrument, Ent Manual Surgical
SINUS DILATION SYSTEM WITH CANNULATED INSTRUMENT
| Applicant | Arthrocare Corp., Austin TX, US |
| Decision | Substantially Equivalent, Oct 4, 2013 |
| Received | Jun 11, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K131709
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.