510(k) K942563 ยท HIR Perineometer
ELITE BIOFEEDBACK
| Applicant | Laborie Medical Technologies, Ltd., South Burlington VT, US |
| Decision | Substantially Equivalent, Jun 6, 1995 |
| Received | May 31, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942563
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.