510(k) K014104 ยท PJE Blood/Plasma Collection Device For Dna Testing
VACUETTE EDTA K2 TUBES
| Applicant | Greiner Vacuette North America, Inc., Baldwin MD, US |
| Decision | Substantially Equivalent, Feb 1, 2002 |
| Received | Dec 13, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K014104
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.