510(k) K101986 ยท DQX Wire, Guide, Catheter
ASAHI ULTIMATEBROS 3 PTCA GUIDE WIRE
| Applicant | Asahi Intecc Co., Ltd., Santa Ana CA, US |
| Decision | Substantially Equivalent, Sep 9, 2011 |
| Received | Jul 14, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101986
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.