510(k) K844161 ยท DQO Catheter, Intravascular, Diagnostic
PTCA GUIDING CATHER
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Jan 2, 1985 |
| Received | Oct 23, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K844161
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.