510(k) K182827 ยท MED Sterilant, Medical Devices
SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model 6900
| Applicant | STERIS Corporation, Mentor OH, US |
| Decision | Substantially Equivalent, Jan 31, 2019 |
| Received | Oct 5, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182827
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.