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FDA 510(k)

IDEAL IQ SOFTWARE OPTION

K-Number: K103411 · 2011-03-22

ApplicantGE Medical Systems
Decision Date2011-03-22
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IDEAL IQ SOFTWARE OPTION is the device name listed in this FDA 510(k) record. The listed applicant is GE Medical Systems. It received FDA 510(k) clearance on 2011-03-22 under 510(k) number K103411. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IDEAL IQ SOFTWARE OPTION?

IDEAL IQ SOFTWARE OPTION is a medical device that received FDA 510(k) clearance on 2011-03-22. The listed applicant is GE Medical Systems. The 510(k) number is K103411.

When did IDEAL IQ SOFTWARE OPTION receive FDA 510(k) clearance?

IDEAL IQ SOFTWARE OPTION received FDA 510(k) clearance on 2011-03-22, under 510(k) number K103411.

Who is the listed applicant for IDEAL IQ SOFTWARE OPTION?

The FDA 510(k) record lists GE Medical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IDEAL IQ SOFTWARE OPTION?

The FDA product code for IDEAL IQ SOFTWARE OPTION is LNH.

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Other records listing GE Medical Systems as applicant

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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.

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