510(k) K791225 ยท DXY Implantable Pacemaker Pulse-Generator
BJORK-SHILEY AORTIC GRAFT VALVE PROSTH
| Applicant | Shiley, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 10, 1979 |
| Received | Jul 3, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791225
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.