510(k) K801885 ยท DTI Sizer, Heart-Valve, Prosthesis
HANCOCK * OBTURATORS
| Applicant | Hancock Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 9, 1980 |
| Received | Aug 7, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801885
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.