510(k) K033478 ยท FMI Needle, Hypodermic, Single Lumen
VACUETTE QUICKSHIELD SAFETY TUBE HOLDER
| Applicant | Greiner Bio-One Vacuette North America, Baldwin MD, US |
| Decision | Substantially Equivalent, Dec 29, 2003 |
| Received | Nov 3, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033478
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.