510(k) K924110 ยท DQI Withdrawal/Infusion Pump
LEOCOR CORFLO PUMP -- MODIFICATION
| Applicant | Leocor, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Sep 1, 1992 |
| Received | Jun 3, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924110
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.