510(k) K230582 ยท MED Sterilant, Medical Devices
SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900
| Applicant | STERIS Corporation, Mentor OH, US |
| Decision | Substantially Equivalent, Mar 28, 2023 |
| Received | Mar 2, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K230582
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.