510(k) K802101 ยท FLN Monitor, Electric For Gravity Flow Infusion Systems
I.V. SENTRY ALARM DEVICE
| Applicant | Pike Medical Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 16, 1980 |
| Received | Sep 3, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802101
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.