510(k) K231179 ยท QJP Catheter, Percutaneous, Neurovasculature
Slinky Catheter
| Applicant | Anoxia Medical, Inc., Hayward CA, US |
| Decision | Substantially Equivalent, Dec 1, 2023 |
| Received | Apr 26, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231179
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.