510(k) K221349 ยท PZI Prescription Use Blood Glucose Meter For Near-Patient Testing
XPER Technology PREMIUM Pro Blood Glucose Monitoring System
| Applicant | Taidoc Technology Corporation, New Taipei City, TW |
| Decision | Substantially Equivalent, Nov 19, 2024 |
| Received | May 9, 2022 |
| Type | Dual Track |
| FDA record | Open on fda.gov |
Recalls that name K221349
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.