510(k) K930286 ยท CBT Arterial Blood Sampling Kit
DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS
| Applicant | Concord/Portex, Keene NH, US |
| Decision | Unknown, Jun 22, 1993 |
| Received | Jan 21, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930286
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.