LOGIQ E10s
K-Number: K200119 · 2020-04-01
Decision Date2020-04-01
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
LOGIQ E10s is a medical device manufactured by GE Medical Systems Ultrasound and Primary Care Diagnostics. It received FDA 510(k) clearance on 2020-04-01 under approval number K200119. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the LOGIQ E10s?
LOGIQ E10s is a medical device that received FDA 510(k) clearance on 2020-04-01. It is manufactured by GE Medical Systems Ultrasound and Primary Care Diagnostics. The 510(k) number is K200119.
When was LOGIQ E10s approved by the FDA?
LOGIQ E10s received FDA 510(k) clearance on 2020-04-01, under approval number K200119.
What company makes LOGIQ E10s?
LOGIQ E10s is manufactured by GE Medical Systems Ultrasound and Primary Care Diagnostics.
What is the FDA product code for LOGIQ E10s?
The FDA product code for LOGIQ E10s is IYN.
Other Devices by GE Medical Systems Ultrasound and Primary Care Diagnostics
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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.