510(k) K093064 ยท NEU Marker, Radiographic, Implantable
TUMARK PROFESSIONAL, MODEL 271560, MR-TUMARK PROFESSIONAL, MODEL 601560
| Applicant | Somatex Medical Technologies GmbH, Cambridge MA, US |
| Decision | Substantially Equivalent, Feb 17, 2010 |
| Received | Sep 30, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093064
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.