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FDA 510(k)

KODAK X-OMATIC IDENT. CAMERA, MODELS 2 AND 2L

K-Number: K870565 · 1987-02-26

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

Device Summary

KODAK X-OMATIC IDENT. CAMERA, MODELS 2 AND 2L 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 K870565. 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 IDENT. CAMERA, MODELS 2 AND 2L?

KODAK X-OMATIC IDENT. CAMERA, MODELS 2 AND 2L 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 K870565.

When did KODAK X-OMATIC IDENT. CAMERA, MODELS 2 AND 2L receive FDA 510(k) clearance?

KODAK X-OMATIC IDENT. CAMERA, MODELS 2 AND 2L received FDA 510(k) clearance on 1987-02-26, under 510(k) number K870565.

Who is the listed applicant for KODAK X-OMATIC IDENT. CAMERA, MODELS 2 AND 2L?

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 IDENT. CAMERA, MODELS 2 AND 2L?

The FDA product code for KODAK X-OMATIC IDENT. CAMERA, MODELS 2 AND 2L 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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