510(k) K042927 ยท PJE Blood/Plasma Collection Device For Dna Testing
VACUETTE EDTA K3 EVACUATED BLOOD COLLECTION TUBES
| Applicant | Greiner Bio-One Vacuette North America, Baldwin MD, US |
| Decision | Substantially Equivalent, Apr 15, 2005 |
| Received | Oct 22, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042927
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.