510(k) K221044 · DRA Catheter, Steerable
AcQGuide® VUE Steerable Sheath
| Applicant | Acutus Medical, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, May 5, 2022 |
| Received | Apr 8, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221044
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.