510(k) K133870 ยท FLN Monitor, Electric For Gravity Flow Infusion Systems
FLUID LEVEL MONITOR
| Applicant | Coleman Laboratories, King Of Prussia PA, US |
| Decision | Substantially Equivalent, Apr 24, 2014 |
| Received | Dec 20, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133870
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.