FDA 510(k) Applications for Medical Device Product Code "NZJ"
(Respirator, N95, For Use By The General Public In Public Health Medical Emergencies)

FDA 510(k) Number Applicant Device Name Decision Date
DEN060009 3M COMPANY 3M N95 HOME RESPIRATOR WITH FLUID RESISTANCE; 3M N95 HOME RESPIRATOR 05/08/2007
K093189 GLAXOSMITHKLINE CONSUMER HEALTHCARE ACTIPROTECT UC N95 RESPIRATOR 07/02/2010
K083176 PASTURE PHARMA PTE LTD PASTURE, MODELS: F550, A520 01/23/2009


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