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FDA 510(k) Applications Submitted by DIOMED, LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K012398
07/27/2001
DIOMED 15 DIODE LASER
DIOMED, LTD.
K051996
07/25/2005
DIOMED DELTA 15, MODEL DELTA 15; DIOMED DELTA 30, MODEL DELTA 30
DIOMED, LTD.
K063828
12/26/2006
DIOMED DELTA 25
DIOMED, LTD.
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