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FDA 510(k)

MAXICAMERA II

K-Number: K770343 · 1977-02-28

ApplicantGeneral Electric Co.
Decision Date1977-02-28
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAXICAMERA II 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 1977-02-28 under 510(k) number K770343. 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 MAXICAMERA II?

MAXICAMERA II is a medical device that received FDA 510(k) clearance on 1977-02-28. The listed applicant is General Electric Co.. The 510(k) number is K770343.

When did MAXICAMERA II receive FDA 510(k) clearance?

MAXICAMERA II received FDA 510(k) clearance on 1977-02-28, under 510(k) number K770343.

Who is the listed applicant for MAXICAMERA II?

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 MAXICAMERA II?

The FDA product code for MAXICAMERA II 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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