510(k) K894574 ยท DHR System, Test, Rheumatoid Factor
TECHNICON DPA-1 SYSTEM RF METHOD
| Applicant | Technicon Instruments Corp., Tarrytown NY, US |
| Decision | Substantially Equivalent, Aug 10, 1989 |
| Received | Jul 21, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894574
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.