510(k) K071691 ยท DXT Injector And Syringe, Angiographic
DUAL SHOT ALPHA
| Applicant | Nemoto Kyorindo Co., Ltd., Laguna Hills CA, US |
| Decision | Substantially Equivalent, Dec 19, 2007 |
| Received | Jun 20, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K071691
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.