510(k) K182405 ยท QDL Integrated Continuous Glucose Monitoring System For Professional Retrospective Use
Dexcom Pro Q Continuous Glucose Monitoring System
| Applicant | Dexcom, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Nov 2, 2018 |
| Received | Sep 4, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182405
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.