510(k) K121902 ยท HIR Perineometer
NATRATONE
| Applicant | Orelle Corporation, Ltd., Seattle WA, US |
| Decision | Substantially Equivalent, Jun 6, 2013 |
| Received | Jun 29, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121902
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.