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FDA 510(k)

KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEM

K-Number: K060079 · 2006-02-08

ApplicantEastman Kodak Company
Decision Date2006-02-08
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Eastman Kodak Company. It received FDA 510(k) clearance on 2006-02-08 under 510(k) number K060079. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEM?

KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEM is a medical device that received FDA 510(k) clearance on 2006-02-08. The listed applicant is Eastman Kodak Company. The 510(k) number is K060079.

When did KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEM receive FDA 510(k) clearance?

KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEM received FDA 510(k) clearance on 2006-02-08, under 510(k) number K060079.

Who is the listed applicant for KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEM?

The FDA 510(k) record lists Eastman Kodak Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEM?

The FDA product code for KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEM is MUH.

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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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