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FDA 510(k)

COMPUTED TOMOGRAPHY X-RAY SYSTEM

K-Number: K903763 · 1990-11-02

ApplicantGeneral Electric Co.
Decision Date1990-11-02
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COMPUTED TOMOGRAPHY X-RAY SYSTEM 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 1990-11-02 under 510(k) number K903763. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPUTED TOMOGRAPHY X-RAY SYSTEM?

COMPUTED TOMOGRAPHY X-RAY SYSTEM is a medical device that received FDA 510(k) clearance on 1990-11-02. The listed applicant is General Electric Co.. The 510(k) number is K903763.

When did COMPUTED TOMOGRAPHY X-RAY SYSTEM receive FDA 510(k) clearance?

COMPUTED TOMOGRAPHY X-RAY SYSTEM received FDA 510(k) clearance on 1990-11-02, under 510(k) number K903763.

Who is the listed applicant for COMPUTED TOMOGRAPHY X-RAY SYSTEM?

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 COMPUTED TOMOGRAPHY X-RAY SYSTEM?

The FDA product code for COMPUTED TOMOGRAPHY X-RAY SYSTEM is JAK.

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Related Devices (Code: JAK)

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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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