510(k) K120119 ยท DQX Wire, Guide, Catheter
SUNMED GUIDE WIRE
| Applicant | Sunny Medical Device (Shenzhen) Co., Ltd., Irvine CA, US |
| Decision | Substantially Equivalent, May 11, 2012 |
| Received | Jan 17, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120119
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.