510(k) K171672 ยท DQY Catheter, Percutaneous
065 Zenith, 074 Zenith
| Applicant | Inneuroco, Inc., Sunrise FL, US |
| Decision | Substantially Equivalent, Oct 19, 2017 |
| Received | Jun 6, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171672
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.