510(k) K852060 ยท FRN Pump, Infusion
INFUSION SETS MODELS 9120,9121,9125, 9122 & 9123
| Applicant | Cardiac Pacemakers, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Jun 7, 1985 |
| Received | May 9, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852060
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.