510(k) K181722 ยท DQO Catheter, Intravascular, Diagnostic
Polyethylene Catheter
| Applicant | Cook Incorporated, Bloomington IN, US |
| Decision | Substantially Equivalent, Mar 22, 2019 |
| Received | Jun 29, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181722
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.