510(k) K923021 ยท KHO Fluorometer, For Clinical Use
AIA-1200DX - AUTOMATED ENZYME IMMUNOASSAY SYSTEM
| Applicant | Tosoh Corp., Washington, D.C. DC, US |
| Decision | Substantially Equivalent, Jul 21, 1992 |
| Received | Jun 23, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923021
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.