510(k) K161546 ยท DQY Catheter, Percutaneous
R2P SlenGuide
| Applicant | Ashitaka Factory of Terumo Corporation, Fujinomiya Shizuoka, JP |
| Decision | Substantially Equivalent, Oct 14, 2016 |
| Received | Jun 3, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161546
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.