510(k) K960703 ยท DHR System, Test, Rheumatoid Factor
RF-LATEX SEIKEN REAGENT SYSTEM
| Applicant | Globe Management Support, Inc., Chuo-Ku, Tokyo 103, JP |
| Decision | Substantially Equivalent, Apr 19, 1996 |
| Received | Feb 20, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960703
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.