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FDA 510(k)

KODAK EKTA-CHEM CLINICAL CHEM. SLIDES

K-Number: K802376 · 1980-10-23

ApplicantEastman Kodak Company
Decision Date1980-10-23
Product CodeCHS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

KODAK EKTA-CHEM CLINICAL CHEM. SLIDES 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 1980-10-23 under 510(k) number K802376. The device is classified under product code CHS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK EKTA-CHEM CLINICAL CHEM. SLIDES?

KODAK EKTA-CHEM CLINICAL CHEM. SLIDES is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is Eastman Kodak Company. The 510(k) number is K802376.

When did KODAK EKTA-CHEM CLINICAL CHEM. SLIDES receive FDA 510(k) clearance?

KODAK EKTA-CHEM CLINICAL CHEM. SLIDES received FDA 510(k) clearance on 1980-10-23, under 510(k) number K802376.

Who is the listed applicant for KODAK EKTA-CHEM CLINICAL CHEM. SLIDES?

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 EKTA-CHEM CLINICAL CHEM. SLIDES?

The FDA product code for KODAK EKTA-CHEM CLINICAL CHEM. SLIDES is CHS.

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Other records listing Eastman Kodak Company as applicant

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Related Devices (Code: CHS)

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.

K926320REFLAB SYSTEM PACK LIQUID CO2 REAGENTMedical Analysis Systems, Inc.K911838ROCHE REAGENT FOR C02Roche Diagnostic Systems, Inc.K860660AMRESCO FLOW PAC CARBON DIOXIDE (CO2) REAGENTSAmresco, Inc.K841080TECHNICON RA-1000 SYS CO2Technicon Instruments Corp.K811257CORNING 965 CARBON DIOXIDE ANALYZERCorning Medical & Scientific

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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