FDA 510(k) Applications Submitted by SUNMAX ENTERPRISE SHANGHAI CO. LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K090336 02/10/2009 SUNMAX ENTERPRISE SHANGHAI CO. POWDER FREE BLUE NITRILE PATIENT EXAMINATION GLOVE TESTED WITH CHEMOTHERAPY DRUGS SUNMAX ENTERPRISE SHANGHAI CO. LTD.
K011717 06/04/2001 SUNMAX BLUE NITRILE POWDERED EXAMINATION GLOVES SUNMAX ENTERPRISE SHANGHAI CO. LTD.
K011765 06/07/2001 SUNMAX BLUE NITRILE POWDER-FREE EXAMINATION GLOVE SUNMAX ENTERPRISE SHANGHAI CO. LTD.
K964964 12/11/1996 POWDER-FREE VINYL PATIENT EXAMINATION GLOVES SUNMAX ENTERPRISE SHANGHAI CO. LTD.
K960746 02/23/1996 SUNMAX ENTERPRISE SHANGHAI VINYL POWDERED PATIENT EXAM. GLOVES SUNMAX ENTERPRISE SHANGHAI CO. LTD.


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