510(k) K883840 ยท LKB Pad, Alcohol, Device Disinfectant
DRI-VENT ARTERIAL BLOOD SAMPLING KIT
| Applicant | Concord Laboratories, Inc., Keene NH, US |
| Decision | Unknown, May 16, 1989 |
| Received | Sep 12, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883840
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.