510(k) K830609 ยท DXT Injector And Syringe, Angiographic
INFLATION DEVICE
| Applicant | Interventional Medical, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Mar 24, 1983 |
| Received | Feb 25, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830609
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.