510(k) K062940 ยท FMI Needle, Hypodermic, Single Lumen
BONE INJECTION GUN (B.I.G.)
| Applicant | Waismed, Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Dec 22, 2006 |
| Received | Sep 28, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062940
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.