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FDA 510(k)

KODAK ECLIPSE IMAGE PROCESSING SOFTWARE

K-Number: K060137 · 2006-03-16

ApplicantEastman Kodak Company
Decision Date2006-03-16
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAK ECLIPSE IMAGE PROCESSING SOFTWARE 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 2006-03-16 under 510(k) number K060137. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK ECLIPSE IMAGE PROCESSING SOFTWARE?

KODAK ECLIPSE IMAGE PROCESSING SOFTWARE is a medical device that received FDA 510(k) clearance on 2006-03-16. The listed applicant is Eastman Kodak Company. The 510(k) number is K060137.

When did KODAK ECLIPSE IMAGE PROCESSING SOFTWARE receive FDA 510(k) clearance?

KODAK ECLIPSE IMAGE PROCESSING SOFTWARE received FDA 510(k) clearance on 2006-03-16, under 510(k) number K060137.

Who is the listed applicant for KODAK ECLIPSE IMAGE PROCESSING SOFTWARE?

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 ECLIPSE IMAGE PROCESSING SOFTWARE?

The FDA product code for KODAK ECLIPSE IMAGE PROCESSING SOFTWARE is MQB.

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Other records listing Eastman Kodak Company as applicant

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K060550KODAK DIRECTVIEW DR 3000 SYSTEM 64KW/80KW GENERATORS, MODELS 6551345, 6551386K060079KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEMK060055KODAK PACSK053347KODAK CARESTREAM PACSK051483KODAK DIRECTVIEW DR SYSTEM DETECTORK051258KODAK DIRECTVIEW DR 7500 SYSTEM, MODEL 8791345

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Related Devices (Code: MQB)

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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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