510(k) K820200 ยท KPE Container, I.V.
IV ALERT SYSTEM
| Applicant | Allied Medical Technologies, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Mar 18, 1982 |
| Received | Jan 26, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820200
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.