K-number	K012505
Device name	SOPRO595 INTRA ORAL CAMERA
Applicant	Sopro
Product code	EIA
Device class	Class I
Decision date	Oct 5, 2001
Decision	Substantially Equivalent
Regulation	872.6640

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View the full FDA submission: accessdata.fda.gov

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SOPRO595 INTRA ORAL CAMERA

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