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FDA 510(k)

CT/T 9800

K-Number: K812241 · 1981-09-09

ApplicantGeneral Electric Co.
Decision Date1981-09-09
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CT/T 9800 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 1981-09-09 under 510(k) number K812241. 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 9800?

CT/T 9800 is a medical device that received FDA 510(k) clearance on 1981-09-09. The listed applicant is General Electric Co.. The 510(k) number is K812241.

When did CT/T 9800 receive FDA 510(k) clearance?

CT/T 9800 received FDA 510(k) clearance on 1981-09-09, under 510(k) number K812241.

Who is the listed applicant for CT/T 9800?

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 9800?

The FDA product code for CT/T 9800 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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