510(k) K950656 ยท IRN Device, Warning, Overload, External Limb, Powered
PED ALERT
| Applicant | Orbitec Technologies Corp., Madison WI, US |
| Decision | Substantially Equivalent, Oct 25, 1995 |
| Received | Feb 13, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950656
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.