510(k) K162382 ยท NBW System, Test, Blood Glucose, Over The Counter
Smart Dongle Blood Glucose Monitoring System
| Applicant | Taidoc Technology Corporation, New Taipei City, TW |
| Decision | Substantially Equivalent, Apr 14, 2017 |
| Received | Aug 24, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162382
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.