510(k) K891041 ยท HDF Speculum, Vaginal, Metal
MIYA SPECULUM
| Applicant | Zinnanti Surgical Instruments, Inc., Chatsworth CA, US |
| Decision | Substantially Equivalent, Mar 22, 1989 |
| Received | Feb 28, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891041
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.