510(k) K983471 ยท DXC Clamp, Vascular
FEMOSTOP COMPRESSION ARCH, FEMOSTOP PUMP, FEMOSTOP BILATERAL ADAPTER
| Applicant | Radi Medical Systems AB, Uppsala, SE |
| Decision | Substantially Equivalent, Feb 23, 1999 |
| Received | Oct 2, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983471
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.