510(k) K230008 · DQK Computer, Diagnostic, Programmable
Ablamap® System
| Applicant | Ablacon, Inc., Denver CO, US |
| Decision | Substantially Equivalent, Jun 8, 2023 |
| Received | Jan 3, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230008
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.