KODAK CINEFLUOROGRAPHIC FILM SO-274
K-Number: K813005 · 1981-11-24
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Device Summary
Frequently Asked Questions
What is the KODAK CINEFLUOROGRAPHIC FILM SO-274?
KODAK CINEFLUOROGRAPHIC FILM SO-274 is a medical device that received FDA 510(k) clearance on 1981-11-24. The listed applicant is Eastman Kodak Company. The 510(k) number is K813005.
When did KODAK CINEFLUOROGRAPHIC FILM SO-274 receive FDA 510(k) clearance?
KODAK CINEFLUOROGRAPHIC FILM SO-274 received FDA 510(k) clearance on 1981-11-24, under 510(k) number K813005.
Who is the listed applicant for KODAK CINEFLUOROGRAPHIC FILM SO-274?
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 CINEFLUOROGRAPHIC FILM SO-274?
The FDA product code for KODAK CINEFLUOROGRAPHIC FILM SO-274 is IWZ.
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: IWZ)
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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