510(k) K013653 ยท HIR Perineometer
INCARE PRESSURE BIOFEEDBACK VAGINAL PRESSURE PROBE AND ANAL PRESSURE PROBE
| Applicant | Hollister, Inc., Libertyville IL, US |
| Decision | Substantially Equivalent, Mar 5, 2002 |
| Received | Nov 6, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013653
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.