510(k) K911868 ยท FPA Set, Administration, Intravascular
INTERLINK(TM) BLUNT CANNULA, MODIFICATION
| Applicant | Baxter Healthcare Corp, Round Lake IL, US |
| Decision | Substantially Equivalent, Jun 24, 1991 |
| Received | Apr 26, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911868
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.