KODAK EKTACHEM CLINICAL CHEMISTRY SLIDE ALCOHOL (ALC)
K-Number: K934273 · 1994-03-21
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Device Summary
Frequently Asked Questions
What is the KODAK EKTACHEM CLINICAL CHEMISTRY SLIDE ALCOHOL (ALC)?
KODAK EKTACHEM CLINICAL CHEMISTRY SLIDE ALCOHOL (ALC) is a medical device that received FDA 510(k) clearance on 1994-03-21. The listed applicant is Eastman Kodak Company. The 510(k) number is K934273.
When did KODAK EKTACHEM CLINICAL CHEMISTRY SLIDE ALCOHOL (ALC) receive FDA 510(k) clearance?
KODAK EKTACHEM CLINICAL CHEMISTRY SLIDE ALCOHOL (ALC) received FDA 510(k) clearance on 1994-03-21, under 510(k) number K934273.
Who is the listed applicant for KODAK EKTACHEM CLINICAL CHEMISTRY SLIDE ALCOHOL (ALC)?
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 ALCOHOL (ALC)?
The FDA product code for KODAK EKTACHEM CLINICAL CHEMISTRY SLIDE ALCOHOL (ALC) is DMT.
Related Clinical Trials
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.
Other records listing Eastman Kodak Company as applicant
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.
Related Devices (Code: DMT)
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.
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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