510(k) K823787 ยท LIB Device, General Purpose, Microbiology, Diagnostic
HANDI-WASH
| Applicant | Dynatech Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 9, 1983 |
| Received | Dec 16, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823787
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.