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FDA 510(k)

KODAK EKTACHEM CLINICAL CHEMISTRY SLIDE PHENYTOIN

K-Number: K941142 · 1994-06-13

ApplicantEastman Kodak Company
Decision Date1994-06-13
Product CodeDIP
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

KODAK EKTACHEM CLINICAL CHEMISTRY SLIDE PHENYTOIN 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 1994-06-13 under 510(k) number K941142. The device is classified under product code DIP. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK EKTACHEM CLINICAL CHEMISTRY SLIDE PHENYTOIN?

KODAK EKTACHEM CLINICAL CHEMISTRY SLIDE PHENYTOIN is a medical device that received FDA 510(k) clearance on 1994-06-13. The listed applicant is Eastman Kodak Company. The 510(k) number is K941142.

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

KODAK EKTACHEM CLINICAL CHEMISTRY SLIDE PHENYTOIN received FDA 510(k) clearance on 1994-06-13, under 510(k) number K941142.

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

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 PHENYTOIN?

The FDA product code for KODAK EKTACHEM CLINICAL CHEMISTRY SLIDE PHENYTOIN is DIP.

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Related Devices (Code: DIP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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