510(k) K052633 ยท DXT Injector And Syringe, Angiographic
DUAL SHOT - CONTRAST DELIVERY SYSTEM
| Applicant | Nemoto Kyorindo Co., Ltd., Tokyo, JP |
| Decision | Substantially Equivalent, Oct 17, 2005 |
| Received | Sep 26, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052633
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.