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FDA 510(k)

QTA PROCESSOR MODULE

K-Number: K840138 · 1984-04-25

ApplicantGeneral Electric Co.
Decision Date1984-04-25
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

QTA PROCESSOR MODULE 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 1984-04-25 under 510(k) number K840138. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QTA PROCESSOR MODULE?

QTA PROCESSOR MODULE is a medical device that received FDA 510(k) clearance on 1984-04-25. The listed applicant is General Electric Co.. The 510(k) number is K840138.

When did QTA PROCESSOR MODULE receive FDA 510(k) clearance?

QTA PROCESSOR MODULE received FDA 510(k) clearance on 1984-04-25, under 510(k) number K840138.

Who is the listed applicant for QTA PROCESSOR MODULE?

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 QTA PROCESSOR MODULE?

The FDA product code for QTA PROCESSOR MODULE is IYO.

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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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