510(k) K233160 ยท DQK Computer, Diagnostic, Programmable
NeuTrace EP Mapping System v.2.1
| Applicant | Anumana, Inc., Cambridge MA, US |
| Decision | Substantially Equivalent, Nov 25, 2023 |
| Received | Sep 27, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233160
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.