510(k) K162233 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
Kurin Blood Culture Collection Set
| Applicant | Pathway, LLC, Santee CA, US |
| Decision | Substantially Equivalent, Dec 23, 2016 |
| Received | Aug 8, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162233
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.