510(k) K160889 ยท NVM Catheter, Angioplasty, Peripheral, Transluminal, Dual-Balloon
BIB Stent Placement Catheter
| Applicant | NuMED, Inc., Hopkinton NY, US |
| Decision | Substantially Equivalent, May 20, 2016 |
| Received | Mar 31, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160889
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.