510(k) K820887 ยท DTI Sizer, Heart-Valve, Prosthesis
MITRAL VALVE ORIFICE SIZER
| Applicant | Celtech, Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 8, 1982 |
| Received | Mar 30, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820887
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.