510(k) K170223 ยท DQO Catheter, Intravascular, Diagnostic
Progreat
| Applicant | Ashitaka Factory of Terumo Corporation, Fujinomiya, JP |
| Decision | Substantially Equivalent, Jul 21, 2017 |
| Received | Jan 25, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170223
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.