510(k) K110193 ยท DXC Clamp, Vascular
FEMOSTOP PLYS, FEMOSTOP HD, FEMOSTOP COMPRESSION ARCH; FEMOSTOP II PLUS SET; FEMOSTOP II PLUS ARCH, BILATERAL ADAPTER; F
| Applicant | St. Jude Medical Systems AB, Uppsala, SE |
| Decision | Substantially Equivalent, Feb 24, 2011 |
| Received | Jan 24, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K110193
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.