510(k) K210737 ยท MED Sterilant, Medical Devices
SYSTEM 1E Liquid Chemical Sterilant Processing System, SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6800, SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900, S40 Sterilant Concentrate
| Applicant | STERIS Corporation, Mentor OH, US |
| Decision | Substantially Equivalent, May 12, 2021 |
| Received | Mar 11, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K210737
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.