510(k) K013612 ยท HIR Perineometer
INCARE PELVIC FLOOR THERAPY SYSTEM
| Applicant | Hollister, Inc., Libertyville IL, US |
| Decision | Substantially Equivalent, Mar 19, 2002 |
| Received | Nov 5, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013612
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.