510(k) K854222 ยท DHR System, Test, Rheumatoid Factor
DIESSE RF TEST KIT
| Applicant | Marvic Interpharma, Inc., Palm Harbor FL, US |
| Decision | Substantially Equivalent, Feb 6, 1986 |
| Received | Oct 18, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854222
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.