510(k) K900879 ยท DYG Catheter, Flow Directed
SOFT-WEDGE(TM) SYRINGE
| Applicant | Baxter Healthcare Corp, Santa Ana CA, US |
| Decision | Substantially Equivalent, May 10, 1990 |
| Received | Feb 26, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900879
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.