510(k) K173956 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
Biowy PlCC Catheter
| Applicant | Biowy Corporation, Lake Forest CA, US |
| Decision | Substantially Equivalent, May 21, 2018 |
| Received | Dec 28, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173956
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.