510(k) K010888 ยท FPA Set, Administration, Intravascular
SIDEPORT PINCH CLAMP DEVICE
| Applicant | Medivice Systems, Ltd., Kfar Saba, IL |
| Decision | Substantially Equivalent, Jun 27, 2001 |
| Received | Mar 23, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010888
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.