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510(k) Data Aggregation

K Number

Device Name

DMS-1000C DERMOABRADER

Manufacturer

AESTHETIC LASERS, INC.

Date Cleared

1996-12-09

(116 days)

Product Code

GFE

Regulation Number

878.4820

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Product Code :

GFE

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized

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Device Description

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