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FDA 510(k)

KODAK EKTASCAN IMAGELINK QUALITY CONTROL WORKSTATI

K-Number: K923270 · 1992-09-11

ApplicantEastman Kodak Company
Decision Date1992-09-11
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAK EKTASCAN IMAGELINK QUALITY CONTROL WORKSTATI 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 1992-09-11 under 510(k) number K923270. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK EKTASCAN IMAGELINK QUALITY CONTROL WORKSTATI?

KODAK EKTASCAN IMAGELINK QUALITY CONTROL WORKSTATI is a medical device that received FDA 510(k) clearance on 1992-09-11. The listed applicant is Eastman Kodak Company. The 510(k) number is K923270.

When did KODAK EKTASCAN IMAGELINK QUALITY CONTROL WORKSTATI receive FDA 510(k) clearance?

KODAK EKTASCAN IMAGELINK QUALITY CONTROL WORKSTATI received FDA 510(k) clearance on 1992-09-11, under 510(k) number K923270.

Who is the listed applicant for KODAK EKTASCAN IMAGELINK QUALITY CONTROL WORKSTATI?

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 EKTASCAN IMAGELINK QUALITY CONTROL WORKSTATI?

The FDA product code for KODAK EKTASCAN IMAGELINK QUALITY CONTROL WORKSTATI is LLZ.

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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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