510(k) K904944 ยท DWX Stripper, Artery, Intraluminal
TRANSLUMINAL ENDARTERECTOMY DEVICE
| Applicant | Baxter Healthcare Corp, Santa Ana CA, US |
| Decision | Substantially Equivalent, Dec 17, 1990 |
| Received | Nov 1, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904944
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.