510(k) K250747 · DQK Computer, Diagnostic, Programmable
Globe® Pulsed Field System
| Applicant | Kardium, Inc., Burnaby, CA |
| Decision | Substantially Equivalent, Jun 25, 2025 |
| Received | Mar 12, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250747
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.