510(k) K063466 ยท FMI Needle, Hypodermic, Single Lumen
TOP FINE
| Applicant | Daejin Tech Medical Manufacturing Co., Ltd., Deer Field IL, US |
| Decision | Substantially Equivalent, Mar 2, 2007 |
| Received | Nov 16, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063466
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.