510(k) K901674 ยท KHO Fluorometer, For Clinical Use
AIA-600 AUTOMATED ENZYME IMMUNOASSAY SYSTEM
| Applicant | Tosoh Corp., Washington, D.C. DC, US |
| Decision | Substantially Equivalent, May 2, 1990 |
| Received | Apr 10, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901674
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.