E-COM DR-2000 DR
K-Number: K193644 · 2020-02-14
ApplicantLivermoretech, Inc.
Decision Date2020-02-14
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
E-COM DR-2000 DR is a medical device manufactured by Livermoretech, Inc.. It received FDA 510(k) clearance on 2020-02-14 under approval number K193644. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the E-COM DR-2000 DR?
E-COM DR-2000 DR is a medical device that received FDA 510(k) clearance on 2020-02-14. It is manufactured by Livermoretech, Inc.. The 510(k) number is K193644.
When was E-COM DR-2000 DR approved by the FDA?
E-COM DR-2000 DR received FDA 510(k) clearance on 2020-02-14, under approval number K193644.
What company makes E-COM DR-2000 DR?
E-COM DR-2000 DR is manufactured by Livermoretech, Inc..
What is the FDA product code for E-COM DR-2000 DR?
The FDA product code for E-COM DR-2000 DR is MQB.
Other Devices by Livermoretech, Inc.
Related Devices (Code: MQB)
K162555EVS 4343, EVS 4343GDRTECH Corporation
K162344INNOLUX RICInnolux Corporation
K161730Wireless Digital Flat Panel DetectorIray Technology (Shanghai) , Ltd.
K162552EVS 3643, EVS 3643GDRTECH Corporation
K163019CareView 750Cw/750C X-ray Flat Panel DetectorsCareray Digital Medical System Co., Ltd.
K160143ClearVision ExamVue Flat Panel DetectorJpi Healthcare, Inc.
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.