510(k) K093473 ยท NEU Marker, Radiographic, Implantable
KMD-MARK1 TISSUE MARKER
| Applicant | Kent Medical Devices, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Jul 2, 2010 |
| Received | Nov 6, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093473
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.