510(k) K903390 ยท DXT Injector And Syringe, Angiographic
MEDRAD MARK V-PLUS INJECTOR
| Applicant | Medrad, Inc., Pittsburgh PA, US |
| Decision | Substantially Equivalent, Sep 26, 1990 |
| Received | Jul 27, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903390
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Dec 14, 2018 | Bayer Medical Care, Inc. MAVIG Portegra or Portegra2 Overhead Counterpoise System (OCS) used in conjunction with the Medrad Stellant CT Injection System (Certegra Workstation), Medrad Mark 7 Arterion" Injection System, or Med Terminated |
DXT | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.