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FDA 510(k) Applications Submitted by SOL WEISS MD INC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K020959
03/25/2002
GLO-SPEC I, II AND III
SOL WEISS MD INC
K012859
08/24/2001
NU-SPEC D
SOL WEISS MD INC
K013817
11/16/2001
GLO-SPEC
SOL WEISS MD INC
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