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FDA 510(k)

KODAK EKTACHEM CLINICAL CHEMISTRY SLIDE HB

K-Number: K854139 · 1985-11-05

ApplicantEastman Kodak Company
Decision Date1985-11-05
Product CodeKHG
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

KODAK EKTACHEM CLINICAL CHEMISTRY SLIDE HB 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 1985-11-05 under 510(k) number K854139. The device is classified under product code KHG. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK EKTACHEM CLINICAL CHEMISTRY SLIDE HB?

KODAK EKTACHEM CLINICAL CHEMISTRY SLIDE HB is a medical device that received FDA 510(k) clearance on 1985-11-05. The listed applicant is Eastman Kodak Company. The 510(k) number is K854139.

When did KODAK EKTACHEM CLINICAL CHEMISTRY SLIDE HB receive FDA 510(k) clearance?

KODAK EKTACHEM CLINICAL CHEMISTRY SLIDE HB received FDA 510(k) clearance on 1985-11-05, under 510(k) number K854139.

Who is the listed applicant for KODAK EKTACHEM CLINICAL CHEMISTRY SLIDE HB?

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 CLINICAL CHEMISTRY SLIDE HB?

The FDA product code for KODAK EKTACHEM CLINICAL CHEMISTRY SLIDE HB is KHG.

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Other records listing Eastman Kodak Company as applicant

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Related Devices (Code: KHG)

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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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