510(k) K093830 ยท DXT Injector And Syringe, Angiographic
MEDLINE ANGIOGRAPHIC CONTROL SYRINGE
| Applicant | Medline Industries, Inc., Mundelein IL, US |
| Decision | Substantially Equivalent, Mar 3, 2011 |
| Received | Dec 14, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093830
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.