FDA 510(k)

GE LOGIQ 9 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL 2404587

K-Number: K040251 · 2004-02-20

ApplicantGe Med. Systems Ultrasound & Prim. Care Diag.,Llc

Decision Date2004-02-20

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

GE LOGIQ 9 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL 2404587 is the device name listed in this FDA 510(k) record. The listed applicant is Ge Med. Systems Ultrasound & Prim. Care Diag.,Llc. It received FDA 510(k) clearance on 2004-02-20 under 510(k) number K040251. 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 9 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL 2404587?

GE LOGIQ 9 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL 2404587 is a medical device that received FDA 510(k) clearance on 2004-02-20. The listed applicant is Ge Med. Systems Ultrasound & Prim. Care Diag.,Llc. The 510(k) number is K040251.

When did GE LOGIQ 9 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL 2404587 receive FDA 510(k) clearance?

GE LOGIQ 9 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL 2404587 received FDA 510(k) clearance on 2004-02-20, under 510(k) number K040251.

Who is the listed applicant for GE LOGIQ 9 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL 2404587?

The FDA 510(k) record lists Ge Med. Systems Ultrasound & Prim. Care Diag.,Llc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GE LOGIQ 9 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL 2404587?

The FDA product code for GE LOGIQ 9 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL 2404587 is IYN.

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Related Devices (Code: IYN)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.