510(k) K821823 ยท FLN Monitor, Electric For Gravity Flow Infusion Systems
I.V. SENTINEL
| Applicant | The John Bunn Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 16, 1982 |
| Received | Jun 22, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821823
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.