510(k) K133016 ยท LRC Instrument, Ent Manual Surgical
VENT-OS SINUS DILATION SYSTEM
| Applicant | Sinusys Corporation, Orinda CA, US |
| Decision | Substantially Equivalent, Dec 9, 2013 |
| Received | Sep 25, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133016
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.