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FDA 510(k)

CLEON IMAGER

K-Number: K770530 · 1977-04-05

ApplicantUnion Carbide Corp.
Decision Date1977-04-05
Product CodeJAM
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CLEON IMAGER 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 1977-04-05 under 510(k) number K770530. The device is classified under product code JAM. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEON IMAGER?

CLEON IMAGER is a medical device that received FDA 510(k) clearance on 1977-04-05. The listed applicant is Union Carbide Corp.. The 510(k) number is K770530.

When did CLEON IMAGER receive FDA 510(k) clearance?

CLEON IMAGER received FDA 510(k) clearance on 1977-04-05, under 510(k) number K770530.

Who is the listed applicant for CLEON IMAGER?

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 IMAGER?

The FDA product code for CLEON IMAGER is JAM.

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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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