510(k) K091188 ยท DQY Catheter, Percutaneous
ASAHI ZENYTEEX GUIDING CATHETER
| Applicant | Asahi Intecc Co., Ltd., Santa Ana CA, US |
| Decision | Substantially Equivalent, Feb 26, 2010 |
| Received | Apr 23, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091188
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.