510(k) K103041 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
VACUETTE BLOOD COLLECTION TUBE WITH LITHIUM HEPARIN AND GEL SEPARATOR
| Applicant | Greiner Bio-One North America, Inc., Baldwin MD, US |
| Decision | Substantially Equivalent, Nov 9, 2010 |
| Received | Oct 14, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K103041
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.