Steris Corporations
Steris Corporations holds FDA 510(k) medical device clearances, first cleared 2018, most recent 2021.
Top product codes for Steris Corporations
Recent clearances by Steris Corporations
- K203630 — BioGuard Air/Water and Suction Valves
- K190104 — SYSTEM 1E Liquid Chemical Sterilant Processing System, SYSTEM 1 Endo Liquid Chemical Sterilant Processing System
- K183295 — Celerity HP Chemical Indicator (CI)
- K183300 — VERIFY V24 Self-Contained Biological Indicator, VERIFY V24 Biological Indicator Challenge Pack
- K182931 — VERIFY All-In-One STEAM Reusable Test Pack, VERIFY All-In-One STEAM Reusable Test Pack with Step Counter, VERIFY All-In-One STEAM Reusable Test Pack with Tracker Tag
- K180342 — SYSTEM 1E Liquid Chemical Sterilant Processing System
- K172748 — VERIFY V24 Self-Contained Biological Indicator, VERIFY V24 Biological Indicator Challenge Pack
Data sourced from openFDA. This site is unofficial and independent of the FDA.