510(k) K873597 ยท DXT Injector And Syringe, Angiographic
TUBING, POLYETHYLENE
| Applicant | Coeur Laboratories, Inc., Raleigh NC, US |
| Decision | Substantially Equivalent, Nov 12, 1987 |
| Received | Sep 4, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873597
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.