510(k) K220272 ยท PZI Prescription Use Blood Glucose Meter For Near-Patient Testing
cobas pulse blood glucose monitoring system
| Applicant | Roche Diagnostics, Indianapolis IN, US |
| Decision | Substantially Equivalent, Apr 26, 2024 |
| Received | Jan 31, 2022 |
| Type | Dual Track |
| FDA record | Open on fda.gov |
Recalls that name K220272
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.