510(k) K962729 ยท DHR System, Test, Rheumatoid Factor
HYCOR HY.TEC/MANUAL RF AUTO-ANTIBODY
| Applicant | Hycor Biomedical, Inc., Garden Grove CA, US |
| Decision | Substantially Equivalent, Mar 7, 1997 |
| Received | Jul 1, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962729
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.