510(k) K811107 ยท FPA Set, Administration, Intravascular
IV SETS
| Applicant | Critikon Company, LLC, Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 12, 1981 |
| Received | Apr 23, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811107
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.