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FDA 510(k) Applications Submitted by DON MORRIS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K960942
02/13/1996
LATEX PATIENT EXAMINATION GLOVE
SIAM SEMPERMED CORP. LTD.
K961415
04/04/1996
LATEX PATIENT EXAMINATION GLOVE (BLUE) (MODIFICATION)
SIAM SEMPERMED CORP. LTD.
K961602
04/04/1996
LATEX PATIENT EXAMINATION GLOVE (PINK)
SIAM SEMPERMED CORP. LTD.
K981975
06/05/1998
LATEX PATIENT EXAMINATION GLOVE POWDERFREE (BLUE COLOR) POLYMER COATED
SIAM SEMPERMED CORP. LTD.
K982885
08/17/1998
PRE-POWDERED NON-STERILE SYNTHETIC EXAMINATION GLOVE
SHANGHAI POSEIDON PLASTIC PRODUCTS CO., LTD.
K983612
10/14/1998
POWDER-FREE NON STERILE VINYL EXAMINATION GLOVES
SHANGHAI JIATAI PLASTIC PRODUCTS CO., LTD.
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