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FDA 510(k) Applications Submitted by JAMES R 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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