510(k) K091022 ยท MED Sterilant, Medical Devices
MODIFICATION TO RESERT XL HLD HIGH LEVEL DISINFECTANT
| Applicant | STERIS Corporation, Mentor OH, US |
| Decision | Substantially Equivalent, Apr 12, 2010 |
| Received | Apr 9, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091022
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.