510(k) K141339 ยท DQX Wire, Guide, Catheter
ASAHI RG3 GUIDEWIRE/ASAHI RG3 SOFT GUIDEWIRE
| Applicant | Asahi Intecc Co., Ltd., Baltimore MD, US |
| Decision | Substantially Equivalent, Oct 23, 2014 |
| Received | May 21, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141339
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.