510(k) K974873 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
VACUETTE (MULTI-USE HOLDER)
| Applicant | Greiner Meditech, Inc., Bel Air MD, US |
| Decision | Substantially Equivalent, Feb 5, 1998 |
| Received | Dec 29, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974873
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.