510(k) K982182 ยท DXC Clamp, Vascular
FEMOSTOP II PLUS DISPOSABLE SET MODEL 11166, FEMOSTOP II PLUS COMPRESSION ARCH MODEL 11168, FEMOSTOP II BILATERAL ADAPT0
| Applicant | Radi Medical Systems AB, Uppsala, SE |
| Decision | Substantially Equivalent, Sep 18, 1998 |
| Received | Jun 22, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982182
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.