510(k) K911270 ยท DQO Catheter, Intravascular, Diagnostic
LEOCOR GUIDING CATHETER
| Applicant | Leocor, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Jan 17, 1992 |
| Received | Mar 22, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911270
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.