510(k) K141707 ยท DQX Wire, Guide, Catheter
ULTRASKIN HYDROPHILIC GUIDE WIRE
| Applicant | Lepu Medical Technology (Beijing) Co., Ltd., South Euclid OH, US |
| Decision | Substantially Equivalent, Jan 21, 2015 |
| Received | Jun 24, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141707
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.