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FDA 510(k)

KODAK MIN-R FAST SCREEN SO-459

K-Number: K860755 · 1986-03-06

ApplicantEastman Kodak Company
Decision Date1986-03-06
Product CodeEAM
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAK MIN-R FAST SCREEN SO-459 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 1986-03-06 under 510(k) number K860755. The device is classified under product code EAM. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK MIN-R FAST SCREEN SO-459?

KODAK MIN-R FAST SCREEN SO-459 is a medical device that received FDA 510(k) clearance on 1986-03-06. The listed applicant is Eastman Kodak Company. The 510(k) number is K860755.

When did KODAK MIN-R FAST SCREEN SO-459 receive FDA 510(k) clearance?

KODAK MIN-R FAST SCREEN SO-459 received FDA 510(k) clearance on 1986-03-06, under 510(k) number K860755.

Who is the listed applicant for KODAK MIN-R FAST SCREEN SO-459?

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 MIN-R FAST SCREEN SO-459?

The FDA product code for KODAK MIN-R FAST SCREEN SO-459 is EAM.

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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: EAM)

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.

K974423ULTRA-VISION MAMMOGRAPHY DETAIL, ULTRA-VISION MAMMOGRAPHY FAST DETAILSterling Diagnostic Imaging, Inc.K963913MD100 & MM150Konica Medical Corp.K954161JPI INTENSIFYING SCREENJpi Healthcare Co, Ltd.K943821KYOKKO SPEC-SERIES INTENSIFY SCREENS-SPEC,SUPER SPECFujifilm Medical System U.S.A., Inc.K943823FUJI FG SERIES INTENSIFYING SCREENS: FG-3-4-8-12Fujifilm Medical System U.S.A., Inc.K943822FUJI UM MAMMO SERIES INTENSIFY SCREENS:Fujifilm Medical System U.S.A., 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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