Kodak Digital Science Film Digitizer L7501/L7506 (with Film Autofeeder)

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K961768 ↗

FDA Product Code

LMA

Device Class

Class II

Regulation

21 CFR Part 892.2030

Advisory Committee

Radiology

FDA Decision

SESE Substantially Equivalent

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  FDA 510(k) K951807 Active Cleared 13 Sep 1995

• Kodak Digital Science(Kds) Medical Image and Information Library

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• Kodak Digital Science Medical Modality Acquisition Unit

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  FDA 510(k) K961739 Active Cleared 14 Nov 1996