510(k) K903495 ยท DXT Injector And Syringe, Angiographic
LIQUID DETECTOR
| Applicant | Life-Tech Intl., Inc., Houston TX, US |
| Decision | Substantially Equivalent, Oct 5, 1990 |
| Received | Aug 3, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903495
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.