K-number	K903329
Device name	CUI ANATOMICAL SILICONE MALAR
Applicant	Cui Corp.
Product code	LZK
Device class	Class II
Decision date	Sep 10, 1990
Decision	Substantially Equivalent
Regulation	878.3550

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View the full FDA submission: accessdata.fda.gov

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CUI ANATOMICAL SILICONE MALAR

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