510(k) K964415 ยท DHR System, Test, Rheumatoid Factor
N-ASSAY TIA RHEUMATOID FACTOR TEST KIT
| Applicant | Kamiya Technology Services, Westport CT, US |
| Decision | Substantially Equivalent, Dec 13, 1996 |
| Received | Oct 1, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964415
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.