510(k) K162523 ยท NZE Hyperthermia Monitor
The IQool System
| Applicant | Braincool AB, Medicon Village, SE |
| Decision | Substantially Equivalent, May 3, 2017 |
| Received | Sep 9, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162523
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.