510(k) K992244 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
GREINER MINICOLLECT COAGULATION BLOOD COLLECTION TUBE
| Applicant | Greiner Meditech, Inc., Bel Air MD, US |
| Decision | Substantially Equivalent, Jul 26, 1999 |
| Received | Jul 2, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992244
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.