510(k) K811432 ยท LDR Controller, Infusion, Intravascular, Electronic
MILLIPORE DUAL RATE INTRAVENOUS CASSETTE
| Applicant | Millipore Corp., Walker MI, US |
| Decision | Substantially Equivalent, Jul 13, 1981 |
| Received | May 22, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811432
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.