510(k) K012043 ยท PJE Blood/Plasma Collection Device For Dna Testing
VACUETTE EDTA K2 GEL TUBES
| Applicant | Greiner Vacuette North America, Inc., Baldwin MD, US |
| Decision | Substantially Equivalent, Sep 24, 2001 |
| Received | Jun 29, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012043
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.