510(k) K882622 ยท JFR Indirect Copper Assay, Ceruloplasmin
CERULOPLASMIN FOR THE TECHNICON DPA-1(TM) SYSTEM
| Applicant | Technicon Instruments Corp., Tarrytown NY, US |
| Decision | Substantially Equivalent, Jul 8, 1988 |
| Received | Jun 24, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882622
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.