510(k) K092896 ยท DXT Injector And Syringe, Angiographic
REMPRESS AND ANGIOGRAPHY CONTRAST DELIVERY SYSTEM REMPRESS
| Applicant | Nemoto Kyorindo Co., Ltd., Kawaguchi-Shi, Saitama, JP |
| Decision | Substantially Equivalent, Oct 29, 2010 |
| Received | Sep 21, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092896
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.