510(k) K160389 ยท DQY Catheter, Percutaneous
NovaCross Microcatheter
| Applicant | Nitiloop , Ltd., Netanya, IL |
| Decision | Substantially Equivalent, Mar 11, 2016 |
| Received | Feb 11, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K160389
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.