510(k) K900350 ยท DXK Echocardiograph
LEOCOR CORFLO(TM) PUMP
| Applicant | Leocor, Inc., Webster TX, US |
| Decision | Substantially Equivalent, Jul 17, 1990 |
| Received | Jan 24, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900350
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.