510(k) K930160 ยท GDM Needle, Aspiration And Injection, Reusable
ILLINOIS STERNAL/ILIAC ASPIRATION NEEDLE
| Applicant | Symbiosis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Jul 6, 1993 |
| Received | Jan 13, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930160
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.