510(k) K072219 ยท NEU Marker, Radiographic, Implantable
CYTOPHIL TISSUE MARKER
| Applicant | Cytophil, Inc., Whitefish Bay WI, US |
| Decision | Substantially Equivalent, Jan 18, 2008 |
| Received | Aug 10, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072219
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.