510(k) K895752 ยท GDM Needle, Aspiration And Injection, Reusable
DIAMOND BLADE SURGICAL KNIVES
| Applicant | Magnum Diamond, Inc., Rapid City SD, US |
| Decision | Substantially Equivalent, Oct 17, 1989 |
| Received | Sep 26, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895752
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.