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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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