510(k) K173450 ยท DXT Injector And Syringe, Angiographic
PRESS DUO elite, PRESS DUO elite AG
| Applicant | Nemoto Kyorindo Co., Ltd., Bunkyo-Ku, JP |
| Decision | Substantially Equivalent, Feb 7, 2018 |
| Received | Nov 6, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173450
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.