510(k) K061483 ยท FMI Needle, Hypodermic, Single Lumen
VACUETTE VISIO PLUS BLOOD COLLECTION NEEDLES
| Applicant | Greiner Bio-One North America, Inc., Baldwin MD, US |
| Decision | Substantially Equivalent, Aug 14, 2006 |
| Received | May 30, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061483
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.