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FDA 510(k)

CLEON 720 LARGE FIELD GAMMA CAMERA

K-Number: K791682 · 1979-12-13

ApplicantUnion Carbide Corp.
Decision Date1979-12-13
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CLEON 720 LARGE FIELD GAMMA CAMERA 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 1979-12-13 under 510(k) number K791682. 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 CLEON 720 LARGE FIELD GAMMA CAMERA?

CLEON 720 LARGE FIELD GAMMA CAMERA is a medical device that received FDA 510(k) clearance on 1979-12-13. The listed applicant is Union Carbide Corp.. The 510(k) number is K791682.

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

CLEON 720 LARGE FIELD GAMMA CAMERA received FDA 510(k) clearance on 1979-12-13, under 510(k) number K791682.

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

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 CLEON 720 LARGE FIELD GAMMA CAMERA?

The FDA product code for CLEON 720 LARGE FIELD GAMMA CAMERA 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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