510(k) K960860 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
GREINER VACUETTE BLOOD COLLECTION TUBE E/EDTA K3
| Applicant | Greiner America, Inc., Wilmington DE, US |
| Decision | Substantially Equivalent, Sep 5, 1996 |
| Received | Mar 1, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960860
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 12, 2023 | Greiner Bio-One North America, Inc. greiner bio-one VACUETTE TUBE 6 ml K3E K3EDTA, 13x100 pink cap-black ring, non-ridged, 24 racks of 50 pcs., 1200 pcs in total, Item #456003 Completed |
JKA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.