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FDA 510(k)

ELECTRIC CT/T OPERATOR DISPLAY CONSOLE

K-Number: K781431 · 1978-09-07

ApplicantGeneral Electric Co.
Decision Date1978-09-07
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ELECTRIC CT/T OPERATOR DISPLAY CONSOLE 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 1978-09-07 under 510(k) number K781431. 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 ELECTRIC CT/T OPERATOR DISPLAY CONSOLE?

ELECTRIC CT/T OPERATOR DISPLAY CONSOLE is a medical device that received FDA 510(k) clearance on 1978-09-07. The listed applicant is General Electric Co.. The 510(k) number is K781431.

When did ELECTRIC CT/T OPERATOR DISPLAY CONSOLE receive FDA 510(k) clearance?

ELECTRIC CT/T OPERATOR DISPLAY CONSOLE received FDA 510(k) clearance on 1978-09-07, under 510(k) number K781431.

Who is the listed applicant for ELECTRIC CT/T OPERATOR DISPLAY CONSOLE?

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 ELECTRIC CT/T OPERATOR DISPLAY CONSOLE?

The FDA product code for ELECTRIC CT/T OPERATOR DISPLAY CONSOLE 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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