510(k) K020972 ยท DHR System, Test, Rheumatoid Factor
WAKO RF-HA (2), RF CALIBRATOR, RF CALIBRATOR SET
| Applicant | Wako Chemicals USA, Inc., Richmond VA, US |
| Decision | Substantially Equivalent, Sep 9, 2002 |
| Received | Mar 26, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020972
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.