FDA 510(k)

GE LOGIQ TWIN

K-Number: K050126 · 2005-02-02

Decision Date2005-02-02

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

GE LOGIQ TWIN is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 2005-02-02 under 510(k) number K050126. 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 GE LOGIQ TWIN?

GE LOGIQ TWIN is a medical device that received FDA 510(k) clearance on 2005-02-02. The listed applicant is General Electric Co.. The 510(k) number is K050126.

When did GE LOGIQ TWIN receive FDA 510(k) clearance?

GE LOGIQ TWIN received FDA 510(k) clearance on 2005-02-02, under 510(k) number K050126.

Who is the listed applicant for GE LOGIQ TWIN?

The FDA 510(k) record lists General Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GE LOGIQ TWIN?

The FDA product code for GE LOGIQ TWIN is IYN.

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Other records listing General Electric Co. as applicant

K103489GE VEO RECONSTRUCTION OPTION K082317GE LUNAR FRAX 10-YEAR FRACTURE RISK SOFTWARE OPTION K081921GE VIVID E9 ULTRASOUND K073297GE LOGIQ P6 K072952GE ECHOPAC K072797GE LOGIQ I COMAPACT ULTRASOUND, GE LOGIQ E COMPACT ULTRASOUND, GE VIVID E COMPACT ULTRASOUND

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Related Devices (Code: IYN)

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.