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FDA 510(k) Applications Submitted by GEORGE Q KUO
FDA 510(k) Number
Submission Date
Device Name
Applicant
K974301
11/17/1997
CLK INT'L. SANITARY LATEX PROBE COVER, CLK ULTRASOUND PROBE COVER
CLK INTL., INC.
K974371
11/20/1997
CLK INT'L POWDER FREE LATEX EXAMINATION GLOVE
CLK INTL., INC.
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