510(k) K193509 ยท DYB Introducer, Catheter
AcQGuide Flex with AcQCross QX, AcQGuide Mini with AcQCross QX
| Applicant | Acutus Medical, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Jan 17, 2020 |
| Received | Dec 18, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K193509
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.