510(k) K003812 ยท FMI Needle, Hypodermic, Single Lumen
VACUETTE SPEEDY QUICK-RELEASE HOLDER
| Applicant | Greiner Vacuette North America, Inc., Baldwin MD, US |
| Decision | Substantially Equivalent, Apr 30, 2001 |
| Received | Dec 11, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003812
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.