SYSTEM 1 endo Liquid Chemical Sterilant Processing System,Model P6900
K-Number: K191343 · 2019-09-05
ApplicantSTERIS Corporation
Decision Date2019-09-05
Product CodeMED
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
SYSTEM 1 endo Liquid Chemical Sterilant Processing System,Model P6900 is a medical device manufactured by STERIS Corporation. It received FDA 510(k) clearance on 2019-09-05 under approval number K191343. 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 P6900?
SYSTEM 1 endo Liquid Chemical Sterilant Processing System,Model P6900 is a medical device that received FDA 510(k) clearance on 2019-09-05. It is manufactured by STERIS Corporation. The 510(k) number is K191343.
When was SYSTEM 1 endo Liquid Chemical Sterilant Processing System,Model P6900 approved by the FDA?
SYSTEM 1 endo Liquid Chemical Sterilant Processing System,Model P6900 received FDA 510(k) clearance on 2019-09-05, under approval number K191343.
What company makes SYSTEM 1 endo Liquid Chemical Sterilant Processing System,Model P6900?
SYSTEM 1 endo Liquid Chemical Sterilant Processing System,Model P6900 is manufactured by STERIS Corporation.
What is the FDA product code for SYSTEM 1 endo Liquid Chemical Sterilant Processing System,Model P6900?
The FDA product code for SYSTEM 1 endo Liquid Chemical Sterilant Processing System,Model P6900 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.