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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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