EzMobile
K-Number: K192098 · 2020-01-20
ApplicantEwoosoft Co., Ltd.
Decision Date2020-01-20
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
EzMobile is a medical device manufactured by Ewoosoft Co., Ltd.. It received FDA 510(k) clearance on 2020-01-20 under approval number K192098. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the EzMobile?
EzMobile is a medical device that received FDA 510(k) clearance on 2020-01-20. It is manufactured by Ewoosoft Co., Ltd.. The 510(k) number is K192098.
When was EzMobile approved by the FDA?
EzMobile received FDA 510(k) clearance on 2020-01-20, under approval number K192098.
What company makes EzMobile?
EzMobile is manufactured by Ewoosoft Co., Ltd..
What is the FDA product code for EzMobile?
The FDA product code for EzMobile is LLZ.
Other Devices by Ewoosoft Co., Ltd.
Related Devices (Code: LLZ)
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.