510(k) K223372 ยท LZG Pump, Infusion, Insulin
Omnipod GO Insulin Delivery Device
| Applicant | Insulet Corporation, Acton MA, US |
| Decision | Substantially Equivalent, Apr 24, 2023 |
| Received | Nov 4, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223372
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.