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FDA 510(k)

GE LOGIQ 500

K-Number: K991611 · 1999-06-09

ApplicantGeneral Electric Co.
Decision Date1999-06-09
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GE LOGIQ 500 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 1999-06-09 under 510(k) number K991611. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GE LOGIQ 500?

GE LOGIQ 500 is a medical device that received FDA 510(k) clearance on 1999-06-09. The listed applicant is General Electric Co.. The 510(k) number is K991611.

When did GE LOGIQ 500 receive FDA 510(k) clearance?

GE LOGIQ 500 received FDA 510(k) clearance on 1999-06-09, under 510(k) number K991611.

Who is the listed applicant for GE LOGIQ 500?

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 500?

The FDA product code for GE LOGIQ 500 is IYO.

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Other records listing General Electric Co. 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.

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Related Devices (Code: IYO)

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.

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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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