510(k) K933712 ยท DHR System, Test, Rheumatoid Factor
EL-RF TEST SYSTEM: EL-RF-IGM KIT
| Applicant | Theratest Laboratories, Inc., Chicago IL, US |
| Decision | Substantially Equivalent, Jan 28, 1994 |
| Received | Jul 30, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933712
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.