510(k) K062608 ยท FMI Needle, Hypodermic, Single Lumen
29G AND 30G K-PACK II NEEDLE
| Applicant | Terumo Europe N.V., Leuven, BE |
| Decision | Substantially Equivalent, Sep 15, 2006 |
| Received | Sep 5, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062608
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.