510(k) K190338 ยท NRY Catheter, Thrombus Retriever
046 Zenith Flex
| Applicant | Inneuroco, Inc., Sunrise FL, US |
| Decision | Substantially Equivalent, Aug 2, 2019 |
| Received | Feb 14, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190338
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.