510(k) K001663 ยท DXT Injector And Syringe, Angiographic
FRONT-LOAD POLYPROPYLENE SYRINGE
| Applicant | Medrad, Inc., Indianola PA, US |
| Decision | Substantially Equivalent, Nov 16, 2000 |
| Received | May 31, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001663
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.