510(k) K922445 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
VACU-PRO
| Applicant | Concord/Portex, Keene NH, US |
| Decision | Substantially Equivalent, Aug 12, 1992 |
| Received | May 22, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922445
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.