LOGIQ F8 Expert, LOGIQ F8, LOGIQ F6
K-Number: K160277 · 2016-03-25
Decision Date2016-03-25
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
LOGIQ F8 Expert, LOGIQ F8, LOGIQ F6 is a medical device manufactured by GE Medical Systems Ultrasound and Primary Care Diagnostics. It received FDA 510(k) clearance on 2016-03-25 under approval number K160277. 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 F8 Expert, LOGIQ F8, LOGIQ F6?
LOGIQ F8 Expert, LOGIQ F8, LOGIQ F6 is a medical device that received FDA 510(k) clearance on 2016-03-25. It is manufactured by GE Medical Systems Ultrasound and Primary Care Diagnostics. The 510(k) number is K160277.
When was LOGIQ F8 Expert, LOGIQ F8, LOGIQ F6 approved by the FDA?
LOGIQ F8 Expert, LOGIQ F8, LOGIQ F6 received FDA 510(k) clearance on 2016-03-25, under approval number K160277.
What company makes LOGIQ F8 Expert, LOGIQ F8, LOGIQ F6?
LOGIQ F8 Expert, LOGIQ F8, LOGIQ F6 is manufactured by GE Medical Systems Ultrasound and Primary Care Diagnostics.
What is the FDA product code for LOGIQ F8 Expert, LOGIQ F8, LOGIQ F6?
The FDA product code for LOGIQ F8 Expert, LOGIQ F8, LOGIQ F6 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.