510(k) K960508 ยท HIR Perineometer
PATHWAY ELECTROMYOGRAPH MODEL PATHWAY II/MR-10/MR-15/MR-20/MR-25
| Applicant | The Prometheus Group, Portsmouth NH, US |
| Decision | Substantially Equivalent, Jan 16, 1997 |
| Received | Feb 5, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960508
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.