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FDA 510(k)

MAXI CAMERA 61

K-Number: K801654 · 1980-08-20

ApplicantGeneral Electric Co.
Decision Date1980-08-20
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAXI CAMERA 61 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 1980-08-20 under 510(k) number K801654. 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 MAXI CAMERA 61?

MAXI CAMERA 61 is a medical device that received FDA 510(k) clearance on 1980-08-20. The listed applicant is General Electric Co.. The 510(k) number is K801654.

When did MAXI CAMERA 61 receive FDA 510(k) clearance?

MAXI CAMERA 61 received FDA 510(k) clearance on 1980-08-20, under 510(k) number K801654.

Who is the listed applicant for MAXI CAMERA 61?

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 MAXI CAMERA 61?

The FDA product code for MAXI CAMERA 61 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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