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FDA 510(k)

GE CT/T 8800 SYSTEM

K-Number: K780326 · 1978-03-14

ApplicantGeneral Electric Co.
Decision Date1978-03-14
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GE CT/T 8800 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 1978-03-14 under 510(k) number K780326. 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 GE CT/T 8800 SYSTEM?

GE CT/T 8800 SYSTEM is a medical device that received FDA 510(k) clearance on 1978-03-14. The listed applicant is General Electric Co.. The 510(k) number is K780326.

When did GE CT/T 8800 SYSTEM receive FDA 510(k) clearance?

GE CT/T 8800 SYSTEM received FDA 510(k) clearance on 1978-03-14, under 510(k) number K780326.

Who is the listed applicant for GE CT/T 8800 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 GE CT/T 8800 SYSTEM?

The FDA product code for GE CT/T 8800 SYSTEM is JAK.

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Other records listing General Electric Co. as applicant

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Related Devices (Code: JAK)

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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