510(k) K190103 ยท MLR Sterilizer, Chemical
V-PRO maX 2 Low Temperature Sterilization System, V-PRO maX Low Temperature Sterilization System, V-PRO 1 Plus Low Temperature Sterilization System, V-PRO 1 Low Temperature Sterilization System
| Applicant | STERIS Corporation, Mentor OH, US |
| Decision | Substantially Equivalent, Apr 5, 2019 |
| Received | Jan 22, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K190103
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.