510(k) K901756 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
INTERJECTOR BLOOD COLLECTION DEVICE
| Applicant | Bowman/Vector, Inc., Fort Lauderdale FL, US |
| Decision | Substantially Equivalent, Aug 29, 1990 |
| Received | Apr 17, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901756
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.