FDA 510(k) Applications Submitted by JAMES MOORE

FDA 510(k) Number Submission Date Device Name Applicant
K093516 11/13/2009 NITRITECH OR MULTIPLE PRIVATE LABEL NON STERILE POWDERED NITRILE EXAMINATION GLOVES SUMMIT GLOVE, INC.
K093517 11/13/2009 NITRITECH OR MULTIPLE PRIVATE LABEL NON-STERILE POWDER FREE NITRILE PATIENT EXAMINATION GLOVE SUMMIT GLOVE, INC.
K970046 01/06/1997 UNIVERSAL LOW PROFILE NASAL HOODS(1250,1275,1350,1450,1475,1550) ACCUTRON, INC.


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