510(k) K991843 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
GREINER MINICOLLECT LITHIUM HEPARIN GEL BLOOD COLLECTION TUBE
| Applicant | Greiner Meditech, Inc., Bel Air MD, US |
| Decision | Substantially Equivalent, Jun 25, 1999 |
| Received | May 28, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991843
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.