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FDA 510(k)

KODAK EKTACHEM 250 ANALYER

K-Number: K922072 · 1992-07-10

ApplicantEastman Kodak Company
Decision Date1992-07-10
Product CodeJJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

KODAK EKTACHEM 250 ANALYER 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 1992-07-10 under 510(k) number K922072. The device is classified under product code JJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK EKTACHEM 250 ANALYER?

KODAK EKTACHEM 250 ANALYER is a medical device that received FDA 510(k) clearance on 1992-07-10. The listed applicant is Eastman Kodak Company. The 510(k) number is K922072.

When did KODAK EKTACHEM 250 ANALYER receive FDA 510(k) clearance?

KODAK EKTACHEM 250 ANALYER received FDA 510(k) clearance on 1992-07-10, under 510(k) number K922072.

Who is the listed applicant for KODAK EKTACHEM 250 ANALYER?

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 EKTACHEM 250 ANALYER?

The FDA product code for KODAK EKTACHEM 250 ANALYER is JJE.

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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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