System 1 endo Liquid Chemical Sterilant Processing System
K-Number: K173256 · 2018-03-02
Device Summary
Frequently Asked Questions
What is the System 1 endo Liquid Chemical Sterilant Processing System?
System 1 endo Liquid Chemical Sterilant Processing System is a medical device that received FDA 510(k) clearance on 2018-03-02. It is manufactured by STERIS Corporation. The 510(k) number is K173256.
When was System 1 endo Liquid Chemical Sterilant Processing System approved by the FDA?
System 1 endo Liquid Chemical Sterilant Processing System received FDA 510(k) clearance on 2018-03-02, under approval number K173256.
What company makes System 1 endo Liquid Chemical Sterilant Processing System?
System 1 endo Liquid Chemical Sterilant Processing System is manufactured by STERIS Corporation.
What is the FDA product code for System 1 endo Liquid Chemical Sterilant Processing System?
The FDA product code for System 1 endo Liquid Chemical Sterilant Processing System is MED.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.