510(k) K810022 ยท JTC Device, Microtiter Diluting/Dispensing
SRD III
| Applicant | Dynatech Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 26, 1981 |
| Received | Jan 5, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810022
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.