510(k) K181546 ยท LRC Instrument, Ent Manual Surgical
Dillard Nasal Balloon Catheter
| Applicant | Intuit Medical Products, LLC, Sugar Hill GA, US |
| Decision | Substantially Equivalent, Jan 3, 2020 |
| Received | Jun 12, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181546
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.