510(k) K944942 ยท GDF Guide, Needle, Surgical
BREAST LESION LOCALIZATION NEEDLE
| Applicant | Promedical , Ltd., Wyckoff NJ, US |
| Decision | Substantially Equivalent, Nov 4, 1994 |
| Received | Oct 7, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K944942
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.