510(k) K161362 ยท DQY Catheter, Percutaneous
ASAHI Corsair Armet
| Applicant | Asahi Intecc Co., Ltd., Hagoya-Shi, JP |
| Decision | Substantially Equivalent, Jun 14, 2016 |
| Received | May 16, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K161362
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.