510(k) K220267 ยท FPA Set, Administration, Intravascular
AMSafe NeuFlo Needleless Connector
| Applicant | Amsino International, Inc., Pomona CA, US |
| Decision | Substantially Equivalent, Oct 7, 2022 |
| Received | Jan 31, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220267
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.