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FDA 510(k)

KODAK EKTASCAN SP CASSETTE

K-Number: K925997 · 1992-12-17

ApplicantEastman Kodak Company
Decision Date1992-12-17
Product CodeIXJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAK EKTASCAN SP CASSETTE 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 1992-12-17 under 510(k) number K925997. The device is classified under product code IXJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK EKTASCAN SP CASSETTE?

KODAK EKTASCAN SP CASSETTE is a medical device that received FDA 510(k) clearance on 1992-12-17. The listed applicant is Eastman Kodak Company. The 510(k) number is K925997.

When did KODAK EKTASCAN SP CASSETTE receive FDA 510(k) clearance?

KODAK EKTASCAN SP CASSETTE received FDA 510(k) clearance on 1992-12-17, under 510(k) number K925997.

Who is the listed applicant for KODAK EKTASCAN SP CASSETTE?

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 EKTASCAN SP CASSETTE?

The FDA product code for KODAK EKTASCAN SP CASSETTE is IXJ.

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Other records listing Eastman Kodak Company as applicant

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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: IXJ)

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.

K964025MITAYA ALUMINUM INTERSPACED X-RAY GRIDX-Ray Accessory Corp.K963893FIBRE INTERSPACED X-RAY GRIDSmit RontgenK962338RADIOGRAPHIC GRIDUnidex Group, Inc.K954294HIGH TRANSMISSION CELLULAR (HTC) GRIDS 18X24 CM & 24X30 CM SIZESThermotrex Corp.K945697SK S-RAY GRIDSSeibu Techno CoprorationK945327JPI X-RAY GRIDJpi America, 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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