EOGas 4 Endo-SteriTest
K-Number: K192980 · 2020-11-12
ApplicantAndersen Sterilizers, Inc.
Decision Date2020-11-12
Product CodeFRC
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
EOGas 4 Endo-SteriTest is a medical device manufactured by Andersen Sterilizers, Inc.. It received FDA 510(k) clearance on 2020-11-12 under approval number K192980. The device is classified under product code FRC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the EOGas 4 Endo-SteriTest?
EOGas 4 Endo-SteriTest is a medical device that received FDA 510(k) clearance on 2020-11-12. It is manufactured by Andersen Sterilizers, Inc.. The 510(k) number is K192980.
When was EOGas 4 Endo-SteriTest approved by the FDA?
EOGas 4 Endo-SteriTest received FDA 510(k) clearance on 2020-11-12, under approval number K192980.
What company makes EOGas 4 Endo-SteriTest?
EOGas 4 Endo-SteriTest is manufactured by Andersen Sterilizers, Inc..
What is the FDA product code for EOGas 4 Endo-SteriTest?
The FDA product code for EOGas 4 Endo-SteriTest is FRC.
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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.