K-number	K963204
Device name	DMS-1000C DERMOABRADER
Applicant	Aesthetic Lasers, Inc.
Product code	GFE
Device class	Class I
Decision date	Dec 9, 1996
Decision	Substantially Equivalent
Regulation	878.4820

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View the full FDA submission: accessdata.fda.gov

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DMS-1000C DERMOABRADER

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