510(k) K181675 ยท PTC Uric Acid Test System For At Home Prescription Use
FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System
| Applicant | Taidoc Technology Corporation, New Taipei City, TW |
| Decision | Substantially Equivalent, Dec 10, 2018 |
| Received | Jun 25, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181675
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.