K-number	K021419
Device name	AART MALAR IMPLANT
Applicant	Aesthetic and Reconstructive Technologies, Inc.
Product code	LZK
Device class	Class II
Decision date	Jul 2, 2002
Decision	Substantially Equivalent
Regulation	878.3550

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View the full FDA submission: accessdata.fda.gov

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AART MALAR IMPLANT

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