EasyOne Filter
K-Number: K221250 · 2022-11-22
ApplicantNdd Medizintechnik AG
Decision Date2022-11-22
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent
Device Summary
EasyOne Filter is a medical device manufactured by Ndd Medizintechnik AG. It received FDA 510(k) clearance on 2022-11-22 under approval number K221250. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the EasyOne Filter?
EasyOne Filter is a medical device that received FDA 510(k) clearance on 2022-11-22. It is manufactured by Ndd Medizintechnik AG. The 510(k) number is K221250.
When was EasyOne Filter approved by the FDA?
EasyOne Filter received FDA 510(k) clearance on 2022-11-22, under approval number K221250.
What company makes EasyOne Filter?
EasyOne Filter is manufactured by Ndd Medizintechnik AG.
What is the FDA product code for EasyOne Filter?
The FDA product code for EasyOne Filter is CAH.
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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.