FDA 510(k) Applications Submitted by SOL WEISS

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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