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FDA 510(k)

CAMERA, CLEON 720 LARGE FIELD GAMMA

K-Number: K790081 · 1979-01-26

ApplicantUnion Carbide Corp.
Decision Date1979-01-26
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CAMERA, CLEON 720 LARGE FIELD GAMMA is the device name listed in this FDA 510(k) record. The listed applicant is Union Carbide Corp.. It received FDA 510(k) clearance on 1979-01-26 under 510(k) number K790081. 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 CAMERA, CLEON 720 LARGE FIELD GAMMA?

CAMERA, CLEON 720 LARGE FIELD GAMMA is a medical device that received FDA 510(k) clearance on 1979-01-26. The listed applicant is Union Carbide Corp.. The 510(k) number is K790081.

When did CAMERA, CLEON 720 LARGE FIELD GAMMA receive FDA 510(k) clearance?

CAMERA, CLEON 720 LARGE FIELD GAMMA received FDA 510(k) clearance on 1979-01-26, under 510(k) number K790081.

Who is the listed applicant for CAMERA, CLEON 720 LARGE FIELD GAMMA?

The FDA 510(k) record lists Union Carbide Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAMERA, CLEON 720 LARGE FIELD GAMMA?

The FDA product code for CAMERA, CLEON 720 LARGE FIELD GAMMA is 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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