510(k) K812233 ยท LDR Controller, Infusion, Intravascular, Electronic
RATEMINDER
| Applicant | Anatros Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 25, 1981 |
| Received | Aug 11, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812233
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.