510(k) K911809 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
NEW-VENT
| Applicant | Concord/Portex, Keene NH, US |
| Decision | Substantially Equivalent, Aug 26, 1991 |
| Received | Apr 23, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911809
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.