510(k) K062168 ยท DXT Injector And Syringe, Angiographic
CONTRAST DELIVERY SYSTEM - DUAL SHOT ALPHA
| Applicant | Nemoto Kyorindo Co., Ltd., Tokyo, JP |
| Decision | Substantially Equivalent, Aug 18, 2006 |
| Received | Jul 31, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062168
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.