510(k) K960430 ยท DXT Injector And Syringe, Angiographic
CONTROL SYRINGE
| Applicant | Scientific Device Manufacturer, LLC, San Rafael CA, US |
| Decision | Substantially Equivalent, Aug 6, 1996 |
| Received | Jan 31, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960430
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.