510(k) K913912 ยท HIR Perineometer
VERIMED PERINEOMETER
| Applicant | Verimed Holdings, Inc., Fort Lauderdale FL, US |
| Decision | Substantially Equivalent, Jun 16, 1992 |
| Received | Aug 29, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913912
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.