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FDA 510(k)

CT/T INDEPENDENT DIAGNOSTIC CENTER

K-Number: K780480 · 1978-04-18

ApplicantGeneral Electric Co.
Decision Date1978-04-18
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CT/T INDEPENDENT DIAGNOSTIC CENTER 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 1978-04-18 under 510(k) number K780480. 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 CT/T INDEPENDENT DIAGNOSTIC CENTER?

CT/T INDEPENDENT DIAGNOSTIC CENTER is a medical device that received FDA 510(k) clearance on 1978-04-18. The listed applicant is General Electric Co.. The 510(k) number is K780480.

When did CT/T INDEPENDENT DIAGNOSTIC CENTER receive FDA 510(k) clearance?

CT/T INDEPENDENT DIAGNOSTIC CENTER received FDA 510(k) clearance on 1978-04-18, under 510(k) number K780480.

Who is the listed applicant for CT/T INDEPENDENT DIAGNOSTIC CENTER?

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 CT/T INDEPENDENT DIAGNOSTIC CENTER?

The FDA product code for CT/T INDEPENDENT DIAGNOSTIC CENTER is 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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