K-number	K933161
Device name	ULTRA-VISION SUPER RAPID INTENSIFYING SCREEN
Applicant	Dupont Medical Products
Product code	EAM
Device class	Class I
Decision date	Oct 7, 1993
Decision	Substantially Equivalent
Regulation	892.1960

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View the full FDA submission: accessdata.fda.gov

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ULTRA-VISION SUPER RAPID INTENSIFYING SCREEN

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