510(k) K900125 ยท FIE Needle, Fistula
ARTERIOVENOUS FISTULA SETS
| Applicant | Baxter Healthcare Corp, Round Lake IL, US |
| Decision | Substantially Equivalent, Jan 31, 1990 |
| Received | Jan 9, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900125
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.