510(k) K931464 ยท LYK Angioscope
BAXTER CORONARY ANGIOSCOPE INFLATION DEVICE
| Applicant | Baxter Healthcare Corp, Irvine CA, US |
| Decision | Substantially Equivalent, Oct 18, 1993 |
| Received | Mar 24, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931464
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.