510(k) K760931 ยท FLN Monitor, Electric For Gravity Flow Infusion Systems
I.V. DRIP MONITOR ALARM DEVICE, MONIFLO
| Applicant | Diemolding Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 5, 1977 |
| Received | Oct 29, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760931
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.