510(k) K861241 ยท DQO Catheter, Intravascular, Diagnostic
ANGIOTOPO CATHETER
| Applicant | Houston Biomedical, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Jan 6, 1987 |
| Received | Apr 2, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861241
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.