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FDA 510(k)

CT/T DATALINK-B7875 AA/B7875 AB

K-Number: K811227 · 1981-07-10

ApplicantGeneral Electric Co.
Decision Date1981-07-10
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CT/T DATALINK-B7875 AA/B7875 AB 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 1981-07-10 under 510(k) number K811227. 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 DATALINK-B7875 AA/B7875 AB?

CT/T DATALINK-B7875 AA/B7875 AB is a medical device that received FDA 510(k) clearance on 1981-07-10. The listed applicant is General Electric Co.. The 510(k) number is K811227.

When did CT/T DATALINK-B7875 AA/B7875 AB receive FDA 510(k) clearance?

CT/T DATALINK-B7875 AA/B7875 AB received FDA 510(k) clearance on 1981-07-10, under 510(k) number K811227.

Who is the listed applicant for CT/T DATALINK-B7875 AA/B7875 AB?

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 DATALINK-B7875 AA/B7875 AB?

The FDA product code for CT/T DATALINK-B7875 AA/B7875 AB 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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