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FDA 510(k)

KODAK EKTACHEM CLIN. CHEM. SLIDES (TRIG)

K-Number: K812029 · 1981-08-03

ApplicantEastman Kodak Company
Decision Date1981-08-03
Product CodeCDT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

KODAK EKTACHEM CLIN. CHEM. SLIDES (TRIG) 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 K812029. The device is classified under product code CDT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

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

KODAK EKTACHEM CLIN. CHEM. SLIDES (TRIG) 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 K812029.

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

KODAK EKTACHEM CLIN. CHEM. SLIDES (TRIG) received FDA 510(k) clearance on 1981-08-03, under 510(k) number K812029.

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

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 (TRIG)?

The FDA product code for KODAK EKTACHEM CLIN. CHEM. SLIDES (TRIG) is CDT.

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Other records listing Eastman Kodak Company as applicant

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Related Devices (Code: CDT)

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.

K133067ADVIA CHEMISTRY TRIGLYCERIDES_2 (TRIG_2) REAGENTSiemens Healthcare Diagnostics, Inc.K130332VITROS CHEMISTRY PRODUCTS TRIG SLIDESOrtho-Clinical Diagnostics, Inc.K113830VANTERA CLINICAL ANALYZERLiposcienceK102993ELITECH CLINICAL SYSTEMS TRIGLYCERIDES SL, ELITECH CLINICAL SYSTEMS CHOLESTEROL SLSeppim S.A.S.K063804OLYMPUS TRIGLYCERIDE TEST SYSTEMOlympus America, Inc.K043546DIMENSION RXL MAX WITH STREAMLAB ANALYTICAL WORKCELL AND SAMPLE TRANSFER MODULEDade Behring, Inc.

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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