510(k) K833520 ยท LDR Controller, Infusion, Intravascular, Electronic
RATEMINDER II SPECIALTY CARE
| Applicant | Anatros Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 22, 1983 |
| Received | Oct 11, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833520
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.