510(k) K011699 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
VACUETTE EVACUATED BLOOD COLLECTION TUBES
| Applicant | Greiner Bio-One Vacuette North America, Baldwin MD, US |
| Decision | Substantially Equivalent, Jun 28, 2001 |
| Received | Jun 1, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011699
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.