510(k) K220258 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
20G Open-System Ally Device Kit (AV100000), 22G Open-System Ally Device Kit (AV110000)
| Applicant | Avia Vascular, Salt Lake City UT, US |
| Decision | Substantially Equivalent, Jul 14, 2022 |
| Received | Jan 31, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220258
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.