FDA 510(k) Applications Submitted by SEMPERMED USA, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K011407 04/19/2001 LATEX POWDER-FREE EXAMINATION GLOVES BLUE, POLYMER COATED, CONTAINS 50 MICROGRAMS OR LESS OF TOTAL WATER EXTRACTABLE PRO SEMPERMED USA, INC.
K011749 05/31/2001 LATEX POWDERED PATIENT EXAMINATION GLOVE, 200 MICROGRAMS OR LESS SEMPERMED USA, INC.


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