510(k) K931517 ยท IRN Device, Warning, Overload, External Limb, Powered
SAFE-STEP
| Applicant | Lenjoy Engineering, Inc., Hawthorne CA, US |
| Decision | Substantially Equivalent, Mar 10, 1995 |
| Received | Mar 26, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931517
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.