510(k) K872774 ยท FRN Pump, Infusion
BETATRON IV SYSTEM
| Applicant | Cardiac Pacemakers, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Jan 5, 1988 |
| Received | Jul 14, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872774
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.