510(k) K010623 ยท LHI Set, I.V. Fluid Transfer
RECONSTITUTION KIT & VIAL CONNECTOR
| Applicant | Bioject, Inc., Portland OR, US |
| Decision | Substantially Equivalent, Apr 5, 2001 |
| Received | Mar 2, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010623
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.