FDA 510(k)

GE LOGIQ 9, MODELS 2188900, 2375600, 2404587 AND 5150000

K-Number: K061129 · 2006-06-01

Decision Date2006-06-01

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

GE LOGIQ 9, MODELS 2188900, 2375600, 2404587 AND 5150000 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 2006-06-01 under 510(k) number K061129. 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, MODELS 2188900, 2375600, 2404587 AND 5150000?

GE LOGIQ 9, MODELS 2188900, 2375600, 2404587 AND 5150000 is a medical device that received FDA 510(k) clearance on 2006-06-01. The listed applicant is General Electric Co.. The 510(k) number is K061129.

When did GE LOGIQ 9, MODELS 2188900, 2375600, 2404587 AND 5150000 receive FDA 510(k) clearance?

GE LOGIQ 9, MODELS 2188900, 2375600, 2404587 AND 5150000 received FDA 510(k) clearance on 2006-06-01, under 510(k) number K061129.

Who is the listed applicant for GE LOGIQ 9, MODELS 2188900, 2375600, 2404587 AND 5150000?

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 9, MODELS 2188900, 2375600, 2404587 AND 5150000?

The FDA product code for GE LOGIQ 9, MODELS 2188900, 2375600, 2404587 AND 5150000 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.