510(k) K023450 ยท NEU Marker, Radiographic, Implantable
BIOPSY SITE TISSUE MARKER DEVICE
| Applicant | Promex, Inc., Franklin IN, US |
| Decision | Substantially Equivalent, Dec 19, 2002 |
| Received | Oct 15, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023450
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.