LOGIQ E10
K-Number: K173555 · 2017-12-20
ApplicantGE Healthcare
Decision Date2017-12-20
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
LOGIQ E10 is a medical device manufactured by GE Healthcare. It received FDA 510(k) clearance on 2017-12-20 under approval number K173555. 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 E10?
LOGIQ E10 is a medical device that received FDA 510(k) clearance on 2017-12-20. It is manufactured by GE Healthcare. The 510(k) number is K173555.
When was LOGIQ E10 approved by the FDA?
LOGIQ E10 received FDA 510(k) clearance on 2017-12-20, under approval number K173555.
What company makes LOGIQ E10?
LOGIQ E10 is manufactured by GE Healthcare.
What is the FDA product code for LOGIQ E10?
The FDA product code for LOGIQ E10 is IYN.
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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.