510(k) K810823 ยท FJK Set, Tubing, Blood, With And Without Anti-Regurgitation Valve
ERIKA EXTENSION SETS
| Applicant | Erika, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Apr 17, 1981 |
| Received | Mar 24, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810823
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.