510(k) K161126 ยท DQY Catheter, Percutaneous
ASAHI Corsair Pro
| Applicant | Asahi Intecc Co., Ltd., Hagoya-Shi, JP |
| Decision | Substantially Equivalent, Aug 25, 2016 |
| Received | Apr 21, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161126
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.