510(k) K971220 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
GREINER VACUETTE BLOOD COLLECTION TUBE
| Applicant | Greiner America, Inc., Lake Mary FL, US |
| Decision | Substantially Equivalent, Jun 4, 1997 |
| Received | Apr 2, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971220
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.