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FDA 510(k)

KODAK 100-J & 100-K CHEMICAL MIXERS

K-Number: K911713 · 1991-06-07

ApplicantEastman Kodak Company
Decision Date1991-06-07
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAK 100-J & 100-K CHEMICAL MIXERS 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 1991-06-07 under 510(k) number K911713. The device is classified under product code IXW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK 100-J & 100-K CHEMICAL MIXERS?

KODAK 100-J & 100-K CHEMICAL MIXERS is a medical device that received FDA 510(k) clearance on 1991-06-07. The listed applicant is Eastman Kodak Company. The 510(k) number is K911713.

When did KODAK 100-J & 100-K CHEMICAL MIXERS receive FDA 510(k) clearance?

KODAK 100-J & 100-K CHEMICAL MIXERS received FDA 510(k) clearance on 1991-06-07, under 510(k) number K911713.

Who is the listed applicant for KODAK 100-J & 100-K CHEMICAL MIXERS?

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 100-J & 100-K CHEMICAL MIXERS?

The FDA product code for KODAK 100-J & 100-K CHEMICAL MIXERS is IXW.

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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.

K060550KODAK DIRECTVIEW DR 3000 SYSTEM 64KW/80KW GENERATORS, MODELS 6551345, 6551386K060137KODAK ECLIPSE IMAGE PROCESSING SOFTWAREK060079KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEMK060055KODAK PACSK053347KODAK CARESTREAM PACSK051483KODAK DIRECTVIEW DR SYSTEM DETECTOR

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Related Devices (Code: IXW)

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.

K111167XTENDER FILM PROCESSOR, SPRINT FILM PROCESSOR MODEL XTENDER MODEL SPRINTVelopex International, Inc.K093503INTRAX FILM PROCESSORVelopex International, Inc.K091628OPTIMAX, COMPACT 2, OPTIMAX 2010, ECOMAXProtec GmbH & Co. KGK024342RADIOGRAPHIC FILM PROCESSOR, MODELS XP400 AND XP1000Daito Co., Ltd.K023801FILM PROCESSOR, MODEL LIFE RAY PRO 1000S.A.I.E.P. S.R.L.K023825FILM PROCESSOR, MODEL LIFE RAY PRO 2500S.A.I.E.P. S.R.L.

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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