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

FDA 510(k) Number Submission Date Device Name Applicant
K993859 11/15/1999 SHANGHAI GLOVMAX ENTERPRISE CO., LTD. PRE-POWDERED VINYL PATIENT EXAMINATION GLOVES SHANGHAI GLOVMAX ENTERPRISE CO.,LTD
K993880 11/15/1999 SHANGHAI GLOVMAX ENTERPRISE CO, LTD., POWDER-FREE VINYL PATIENT EXAMINATION GLOVES SHANGHAI GLOVMAX ENTERPRISE CO.,LTD
K021000 03/28/2002 SHANGHAI GLOVMAX ENTERPRISE POWDERED BLUE NITRILE EXAMINATION GLOVES SHANGHAI GLOVMAX ENTERPRISE CO.,LTD
K021001 03/28/2002 SHANGHAI GLOVMAX ENTERPRISE POWDERFREE BLUE NITRILE EXAMINATION GLOVES SHANGHAI GLOVMAX ENTERPRISE CO.,LTD


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact