FDA 510(k) Application Details - K963204

Device Classification Name Brush, Dermabrasion, Powered

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510(K) Number K963204
Device Name Brush, Dermabrasion, Powered
Applicant AESTHETIC LASERS, INC.
528 COLLEGE PKWY., SUITE C-1
ANNAPOLIS, MD 21401 US
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Contact FRED DE JACMA
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Regulation Number 878.4820

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Classification Product Code GFE
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Date Received 08/15/1996
Decision Date 12/09/1996
Decision SESE - SUBST EQUIV
Classification Advisory Committee SU - General & Plastic Surgery
Review Advisory Committee SU - General & Plastic Surgery
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review



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