510(k) K820043 ยท LIB Device, General Purpose, Microbiology, Diagnostic
TEK-PRO TEK-TATOR V ROTATOR & HUMIDIFY
| Applicant | American Dade, Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 28, 1982 |
| Received | Jan 7, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820043
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.