510(k) K800191 ยท HIR Perineometer
PERITONE
| Applicant | Laurie Ann Kaiser, Ph.D., Walker MI, US |
| Decision | Substantially Equivalent, Apr 16, 1980 |
| Received | Jan 29, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800191
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.