K-number	K100919
Device name	PRO FOCUS 2202, PRO FOCUS 2202 UV MODEL: TYPE 2202
Applicant	B-K Medical Aps
Product code	IYN
Device class	Class II
Decision date	Dec 16, 2011
Decision	Substantially Equivalent
Regulation	892.1550

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View the full FDA submission: accessdata.fda.gov

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PRO FOCUS 2202, PRO FOCUS 2202 UV MODEL: TYPE 2202

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