510(k) K955034 ยท IRN Device, Warning, Overload, External Limb, Powered
FORCEGUARD
| Applicant | Impact Monitors, Inc., Longmont CO, US |
| Decision | Substantially Equivalent, Apr 10, 1996 |
| Received | Nov 2, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955034
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.