510(k) K792241 ยท IRN Device, Warning, Overload, External Limb, Powered
PELIMIT
| Applicant | Colmed, Ltd., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 30, 1979 |
| Received | Nov 7, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792241
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.