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FDA 510(k) Applications for Medical Device Product Code "NZJ"
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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 |