510(k) K830235 ยท GDM Needle, Aspiration And Injection, Reusable
FRANZEN NEEDLE GUIDE
| Applicant | Precision Dynamics Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 23, 1983 |
| Received | Jan 25, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830235
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.