510(k) K002777 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
VACUETTE WITH PPACK
| Applicant | Greiner Vacuette North America, Inc., Ellicott City MD, US |
| Decision | Substantially Equivalent, Oct 5, 2000 |
| Received | Sep 6, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002777
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.