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FDA 510(k)

KODAK EKTACHEM CLIN. CHEM. SLIDES (TP)

K-Number: K812028 · 1981-08-03

Decision Date1981-08-03
Product CodeCEK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

KODAK EKTACHEM CLIN. CHEM. SLIDES (TP) 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 1981-08-03 under 510(k) number K812028. The device is classified under product code CEK. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK EKTACHEM CLIN. CHEM. SLIDES (TP)?

KODAK EKTACHEM CLIN. CHEM. SLIDES (TP) is a medical device that received FDA 510(k) clearance on 1981-08-03. The listed applicant is Eastman Kodak Company. The 510(k) number is K812028.

When did KODAK EKTACHEM CLIN. CHEM. SLIDES (TP) receive FDA 510(k) clearance?

KODAK EKTACHEM CLIN. CHEM. SLIDES (TP) received FDA 510(k) clearance on 1981-08-03, under 510(k) number K812028.

Who is the listed applicant for KODAK EKTACHEM CLIN. CHEM. SLIDES (TP)?

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 CLIN. CHEM. SLIDES (TP)?

The FDA product code for KODAK EKTACHEM CLIN. CHEM. SLIDES (TP) is CEK.

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.

View all 238 devices →

Related Devices (Code: CEK)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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