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FDA 510(k)

DATA CAMERA

K-Number: K780491 · 1978-04-18

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

Device Summary

DATA CAMERA 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 K780491. The device is classified under product code IYX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DATA CAMERA?

DATA CAMERA 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 K780491.

When did DATA CAMERA receive FDA 510(k) clearance?

DATA CAMERA received FDA 510(k) clearance on 1978-04-18, under 510(k) number K780491.

Who is the listed applicant for DATA CAMERA?

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 DATA CAMERA?

The FDA product code for DATA CAMERA is IYX.

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Related Devices (Code: IYX)

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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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