FDA 510(k) Applications Submitted by JOSEPH NEUSER

FDA 510(k) Number Submission Date Device Name Applicant
K070760 03/20/2007 POWDER FREE CHLORINATED LATEX PATIENT EXAMINATION GLOVE DERMA CARE PLUS PRODUCTS LLC
K111589 06/07/2011 POWDER FREE NITRILE PATIENT EXAMINATION GLOVE WITH COLLOIDAL OATMEAL USP A SKIN PROTECTANT DRUG DERMA CARE PLUS PRODUCTS, LLC
K955424 11/28/1995 OSTAR ULTRAVENA INDUSTRIES, LTD.


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