510(k) K080704 ยท FLN Monitor, Electric For Gravity Flow Infusion Systems
LOW FLUID ALARM
| Applicant | Em-Tec GmbH, Finning, Bavaria, DE |
| Decision | Substantially Equivalent, Apr 17, 2008 |
| Received | Mar 12, 2008 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K080704
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.