510(k) K780223 ยท FLN Monitor, Electric For Gravity Flow Infusion Systems
PARENTERAL INFUSION CONTROLLER
| Applicant | Travenol Laboratories, S.A., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 10, 1978 |
| Received | Feb 9, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780223
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.