510(k) K844556 ยท FLN Monitor, Electric For Gravity Flow Infusion Systems
KHM 2000 DRIP WATCHER
| Applicant | The Timeter Group, Lancaster PA, US |
| Decision | Substantially Equivalent, Jan 14, 1985 |
| Received | Nov 21, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K844556
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.