K-number	K875312
Device name	UFR DIGITAL RETROFIT
Applicant	Yankee Intl. Medical Research & Mfg., Ltd.
Product code	FJB
Device class	Class II
Decision date	Feb 19, 1988
Decision	Substantially Equivalent
Regulation	876.5820

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View the full FDA submission: accessdata.fda.gov

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UFR DIGITAL RETROFIT

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