510(k) K971712 ยท DXT Injector And Syringe, Angiographic
COEUR 130 ML ANGIOGRAPHIC SYRINGE
| Applicant | Coeur Laboratories, Inc., Raleigh NC, US |
| Decision | Substantially Equivalent, Oct 8, 1997 |
| Received | May 9, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971712
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.