510(k) K874151 ยท DHR System, Test, Rheumatoid Factor
RF DIPSTICK TEST KIT
| Applicant | Lipogen, Inc., Knoxville TN, US |
| Decision | Substantially Equivalent, Dec 29, 1987 |
| Received | Oct 13, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874151
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.