510(k) K962591 ยท IRN Device, Warning, Overload, External Limb, Powered
FOOT WEIGHT ALARM
| Applicant | Cleveland Medical Devices, Inc., Cleveland OH, US |
| Decision | Substantially Equivalent, Dec 4, 1996 |
| Received | Jul 2, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962591
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.