510(k) K033802 ยท DHR System, Test, Rheumatoid Factor
ATHENA MULTI-LITE RHEUMATOID FACTOR IGM TEST SYSTEM
| Applicant | Zeus Scientific, Inc., Branchburg NJ, US |
| Decision | Substantially Equivalent, Feb 27, 2004 |
| Received | Dec 8, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033802
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.