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FDA 510(k) Applications Submitted by ALAN BUNTING
FDA 510(k) Number
Submission Date
Device Name
Applicant
K970143
01/15/1997
C4
CLINICON CORP.
K040121
01/20/2004
DERMAWAVE 5000 COMBI MAX SYSTEM
DERMAWAVE, LLC
K962242
06/11/1996
SURESCAN
CLINICON CORP.
K964831
12/02/1996
SURESCAN
CLINICON CORP.
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