510(k) K881730 ยท GDM Needle, Aspiration And Injection, Reusable
BREAST LOCALIZATION NEEDLES
| Applicant | Hart Enterprises, Inc., Wyoming MI, US |
| Decision | Substantially Equivalent, May 13, 1988 |
| Received | Apr 22, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881730
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.