510(k) K011688 ยท HIR Perineometer
PELVICFLEXER EXERCISE DEVICE
| Applicant | Pelvicflex, Inc., Great Neck NY, US |
| Decision | Substantially Equivalent, Mar 20, 2002 |
| Received | May 31, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011688
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.