510(k) K802826 ยท JHX Fluorometric Method, Cpk Or Isoenzymes
PARAGON ELECTRO. CREATINE KINASE TEST KI
| Applicant | Beckman Instruments, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 9, 1981 |
| Received | Nov 10, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802826
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.