510(k) K874928 ยท GDM Needle, Aspiration And Injection, Reusable
WHOLEY (TM) BIOPSY DEVICE
| Applicant | Medrad, Inc., Pittsburgh PA, US |
| Decision | Substantially Equivalent, Dec 30, 1987 |
| Received | Dec 2, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874928
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.