510(k) K141893 ยท HIR Perineometer
VIBRANCE KEGEL DEVICE (VKD)
| Applicant | Bioinfinity (M) Sdn. Bhd., Austin TX, US |
| Decision | Substantially Equivalent, Dec 18, 2014 |
| Received | Jul 14, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141893
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.