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FDA 510(k) Applications Submitted by DIOMED, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K013499
10/22/2001
DIOMED 15 PLUS AND DIOMED 30PLUS LASERS
DIOMED, INC.
K990014
01/04/1999
DIOSCAN
DIOMED, INC.
K000982
03/27/2000
A100 AESTHETIC DIODE LASER
DIOMED, INC.
K041957
07/21/2004
EVLT KIT AND THE D15PLUS AND D30PLUS DIODE LASERS
DIOMED, INC.
K023543
10/22/2002
EVLT KIT AND D15PLUS AND D30PLUS DIODE
DIOMED, INC.
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