510(k) K862030 ยท DQO Catheter, Intravascular, Diagnostic
POLY-TECH ANGIOGRAPHY CATHETER
| Applicant | Poly-Tech Medical Device Research & Development, Alvin TX, US |
| Decision | Substantially Equivalent, Aug 8, 1986 |
| Received | May 28, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862030
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.