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FDA 510(k)

IQ SYSTEM

K-Number: K922218 · 1992-12-08

Decision Date1992-12-08
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

IQ SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Renaissance Technology, Inc.. It received FDA 510(k) clearance on 1992-12-08 under 510(k) number K922218. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IQ SYSTEM?

IQ SYSTEM is a medical device that received FDA 510(k) clearance on 1992-12-08. The listed applicant is Renaissance Technology, Inc.. The 510(k) number is K922218.

When did IQ SYSTEM receive FDA 510(k) clearance?

IQ SYSTEM received FDA 510(k) clearance on 1992-12-08, under 510(k) number K922218.

Who is the listed applicant for IQ SYSTEM?

The FDA 510(k) record lists Renaissance Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IQ SYSTEM?

The FDA product code for IQ SYSTEM is DXG.

Related Clinical Trials

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.

Other records listing Renaissance Technology, Inc. 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.

Related Devices (Code: DXG)

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.

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.

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