510(k) K152361 ยท IZQ Injector, Contrast Medium, Automatic
OptiOne Single-Head Contrast Delivery System with Pedestal; with Ceiling Suspension;Injector, OptiOne Base System
| Applicant | Liebel-Flarsheim Company, LLC, Cincinnati OH, US |
| Decision | Substantially Equivalent, Jan 14, 2016 |
| Received | Aug 20, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152361
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.