LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3
K-Number: K161224 · 2016-08-05
Device Summary
Frequently Asked Questions
What is the LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3?
LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3 is a medical device that received FDA 510(k) clearance on 2016-08-05. The listed applicant is GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC. The 510(k) number is K161224.
When did LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3 receive FDA 510(k) clearance?
LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3 received FDA 510(k) clearance on 2016-08-05, under 510(k) number K161224.
Who is the listed applicant for LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3?
The FDA 510(k) record lists GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3?
The FDA product code for LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3 is IYN.
Other records listing GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: IYN)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.