SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model 6900
K-Number: K182827 · 2019-01-31
ApplicantSTERIS Corporation
Decision Date2019-01-31
Product CodeMED
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model 6900 is a medical device manufactured by STERIS Corporation. It received FDA 510(k) clearance on 2019-01-31 under approval number K182827. The device is classified under product code MED. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model 6900?
SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model 6900 is a medical device that received FDA 510(k) clearance on 2019-01-31. It is manufactured by STERIS Corporation. The 510(k) number is K182827.
When was SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model 6900 approved by the FDA?
SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model 6900 received FDA 510(k) clearance on 2019-01-31, under approval number K182827.
What company makes SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model 6900?
SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model 6900 is manufactured by STERIS Corporation.
What is the FDA product code for SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model 6900?
The FDA product code for SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model 6900 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.