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FDA 510(k)

KODAK X-OMATIC IDENTIFICATION CAMERA DIGITAL

K-Number: K870701 · 1987-02-26

ApplicantEastman Kodak Company
Decision Date1987-02-26
Product CodeJAC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAK X-OMATIC IDENTIFICATION CAMERA DIGITAL 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 1987-02-26 under 510(k) number K870701. The device is classified under product code JAC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK X-OMATIC IDENTIFICATION CAMERA DIGITAL?

KODAK X-OMATIC IDENTIFICATION CAMERA DIGITAL is a medical device that received FDA 510(k) clearance on 1987-02-26. The listed applicant is Eastman Kodak Company. The 510(k) number is K870701.

When did KODAK X-OMATIC IDENTIFICATION CAMERA DIGITAL receive FDA 510(k) clearance?

KODAK X-OMATIC IDENTIFICATION CAMERA DIGITAL received FDA 510(k) clearance on 1987-02-26, under 510(k) number K870701.

Who is the listed applicant for KODAK X-OMATIC IDENTIFICATION CAMERA DIGITAL?

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 X-OMATIC IDENTIFICATION CAMERA DIGITAL?

The FDA product code for KODAK X-OMATIC IDENTIFICATION CAMERA DIGITAL is JAC.

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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: JAC)

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.

K942883DIGITAL I.D. CAMERAMiles Inc., Agfa DivisionK930752CT/MRI TOPOGRAPHIC MARKERI.Z.I. Corp.K932357FUJI EC ID CAMERAFujifilm Medical System U.S.A., Inc.K925892SOLSTICE XRAY RING MARKER PADSolstice Corp.K923533ADMARKPlanmeca USA, Inc.K926404KODAK X-OMATIC IDENTIFICATION CAMERA, MODEL 4 & 4LEastman Kodak Company

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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