LOGIQ e
K-Number: K260398 · 2026-05-26
Device Summary
Frequently Asked Questions
What is the LOGIQ e?
LOGIQ e is a medical device that received FDA 510(k) clearance on 2026-05-26. The listed applicant is GE Medical Systems Ultrasound and Primary Care Diagnostics. The 510(k) number is K260398.
When did LOGIQ e receive FDA 510(k) clearance?
LOGIQ e received FDA 510(k) clearance on 2026-05-26, under 510(k) number K260398.
Who is the listed applicant for LOGIQ e?
The FDA 510(k) record lists GE Medical Systems Ultrasound and Primary Care Diagnostics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LOGIQ e?
The FDA product code for LOGIQ e is IYN.
Other records listing GE Medical Systems Ultrasound and Primary Care Diagnostics 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.