510(k) K023305 ยท HIR Perineometer
KEGELMASTER 2000
| Applicant | Kegelmaster 2000 , Ltd., Crofton MD, US |
| Decision | Substantially Equivalent, Dec 26, 2002 |
| Received | Oct 3, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023305
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.