510(k) K212988 ยท MMX Device, Percutaneous Retrieval
ONO Retrieval Device
| Applicant | Onocor Vascular, LLC, West Chester PA, US |
| Decision | Substantially Equivalent, May 23, 2022 |
| Received | Sep 20, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212988
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.