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FDA 510(k)

KODATROL LIQUID CONTROL LEVELS I & II

K-Number: K903189 · 1990-08-22

ApplicantEastman Kodak Company
Decision Date1990-08-22
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

KODATROL LIQUID CONTROL LEVELS I & II 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 1990-08-22 under 510(k) number K903189. The device is classified under product code DIF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODATROL LIQUID CONTROL LEVELS I & II?

KODATROL LIQUID CONTROL LEVELS I & II is a medical device that received FDA 510(k) clearance on 1990-08-22. The listed applicant is Eastman Kodak Company. The 510(k) number is K903189.

When did KODATROL LIQUID CONTROL LEVELS I & II receive FDA 510(k) clearance?

KODATROL LIQUID CONTROL LEVELS I & II received FDA 510(k) clearance on 1990-08-22, under 510(k) number K903189.

Who is the listed applicant for KODATROL LIQUID CONTROL LEVELS I & II?

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 KODATROL LIQUID CONTROL LEVELS I & II?

The FDA product code for KODATROL LIQUID CONTROL LEVELS I & II is DIF.

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Other records listing Eastman Kodak Company as applicant

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Related Devices (Code: DIF)

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.

K153474Detectabuse Liquid Control Urine, Detectabuse Stat-Skreen Liquid Control Urine, Detectabuse Liquid Control Urine, AU/NZ, Detectabuse Liquid Control Urine, Immunoassay Series, Detectabuse Liquid Control Urine, GC/MS and Confirm seriesBiochemical Diagnostics, Inc.K132688SALIVABUSE LIQUID ORAL FLUID CONTROL, SALIVABUSE LIQUID ORAL FLUID CONTROL, AU/NZBiochemical Diagnostics, Inc.K132174MULTICHEM WBTTechno-Path Manufacturing , Ltd.K121122DETECTABUSE LIQUID CONTROL, DETECTABUSE STAT-SKREEN LIQUID CONTROLBiochemical Diagnostic, Inc.K121143LIQUICHEK WHOLE BLOOD IMMUNOSUPPRESSANT CONTROL TILEVEL (1,2 AND 3)Bio-Rad LaboratoriesK120504LIQUICHEK URINE TOXICOLOGY CONTROL, S10 & S10 MINIPAK, LIQUICHEK URINE TOXICOLOGY CONTROL, LEVEL S20 & LEVEL S20 MINIPAKBio-Rad Laboratories, Inc.

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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