Ultra-Vision Super Rapid Intensifying Screen

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

510(k) Number

K933161 ↗

FDA Product Code

EAM

Device Class

Class I

Regulation

21 CFR Part 892.1960

Advisory Committee

Radiology

FDA Decision

SESE Substantially Equivalent

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See all devices from Dupont Medical Products →