510(k) K924270 ยท GDF Guide, Needle, Surgical
BREAST LESION LOCALIZATION NEEDLE
| Applicant | Core Medical, Inc., Concord NC, US |
| Decision | Substantially Equivalent, Sep 23, 1992 |
| Received | Aug 24, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924270
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.