FDA 510(k) Applications Submitted by GLAXOSMITHKLINE CONSUMER HEALTHCARE

FDA 510(k) Number Submission Date Device Name Applicant
K093189 10/09/2009 ACTIPROTECT UC N95 RESPIRATOR GLAXOSMITHKLINE CONSUMER HEALTHCARE
K081923 07/07/2008 ACTIPROTECT UF N95 RESPIRATOR, DOUBLE STRAP, FLAT FOLD GLAXOSMITHKLINE CONSUMER HEALTHCARE
K093161 10/06/2009 ACTIPROTECT UF N95 RESPIRATOR GLAXOSMITHKLINE CONSUMER HEALTHCARE


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