510(k) K960858 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
GREINER VACUTTE BLOOD COLLECTION TUBE W/ CLOT ACTIVATOR & GEL SEPARATOR
| Applicant | Greiner America, Inc., Wilmington DE, US |
| Decision | Substantially Equivalent, Aug 30, 1996 |
| Received | Mar 1, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960858
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 17, 2024 | Greiner Bio-One North America, Inc. VACUETTE TUBE 8 ml CAT Serum Separator Clot Activator 16x100
red cap-yellow ring, non-ridged Open, Classified |
JKA | None listed |
| Oct 22, 2005 | Greiner VACUETTE North America Serum Blood Collection Tubes Terminated |
JKA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.