510(k) K963012 ยท LHI Set, I.V. Fluid Transfer
BIOJECT NEEDLE-FREE VIAL ADAPTER (13MM)
| Applicant | Bioject, Inc., Portland OR, US |
| Decision | Substantially Equivalent, Oct 15, 1996 |
| Received | Aug 2, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963012
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.