510(k) K945611 ยท HIR Perineometer
PERITRON
| Applicant | Cardio Design Pty. , Ltd., Eden Prairie MN, US |
| Decision | Substantially Equivalent, Feb 8, 1996 |
| Received | Nov 15, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945611
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.