510(k) K210110 ยท DQY Catheter, Percutaneous
Guidion
| Applicant | Imds Operations B.V., Roden, NL |
| Decision | Substantially Equivalent, Mar 31, 2021 |
| Received | Jan 19, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210110
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.