510(k) K171217 ยท DXT Injector And Syringe, Angiographic
DyeVert Plus Contrast Reduction System, DyeVert NG Contrast Reduction System
| Applicant | Osprey Medical, Inc., Minnetonka MN, US |
| Decision | Substantially Equivalent, May 26, 2017 |
| Received | Apr 26, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K171217
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.