510(k) K191832 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
Kurin Blood Culture Collection Set with Kurin Lock Technology, Push-Button Needle (Product models M-21221, M-21223, D-21221, D-21223, T-21221, T-21223)
| Applicant | Kurin, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Feb 4, 2020 |
| Received | Jul 9, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191832
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.