510(k) K002617 ยท HIR Perineometer
PERIFORM PERINEOMETRIC PROBE, MODEL 8300
| Applicant | Neen Design , Ltd., Dereham, Norfolk, GB |
| Decision | Substantially Equivalent, Apr 5, 2001 |
| Received | Aug 23, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002617
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.