510(k) K191343 ยท MED Sterilant, Medical Devices
SYSTEM 1 endo Liquid Chemical Sterilant Processing System,Model P6900
| Applicant | STERIS Corporation, Mentor OH, US |
| Decision | Substantially Equivalent, Sep 5, 2019 |
| Received | May 20, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K191343
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.