510(k) K162373 ยท KRD Device, Vascular, For Promoting Embolization
LC Bead LUMI
| Applicant | Biocompatibles UK Limited, Farnham, GB |
| Decision | Substantially Equivalent, Dec 16, 2016 |
| Received | Aug 24, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162373
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.