510(k) K133990 ยท HIR Perineometer
IEVA REHABILITATIVE POSITIONAL DEVICE
| Applicant | Remendium Labs, LLC, Baton Rouge LA, US |
| Decision | Substantially Equivalent, Oct 9, 2014 |
| Received | Dec 27, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133990
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.