510(k) K223874 ยท KDN System, Perfusion, Kidney
BAROguard
| Applicant | Paragonix Technologies, Braintree MA, US |
| Decision | Substantially Equivalent, Aug 15, 2023 |
| Received | Dec 23, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223874
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.