FDA 510(k) Applications Submitted by SHANGHAI SUPER GLOVES CO., LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K974120 10/31/1997 POWDER-FREE VINYL PATIENT EXAMINATION GLOVES SHANGHAI SUPER GLOVES CO., LTD.
K974151 11/04/1997 VINYL PATIENT EXAMINATION GLOVES (POWDERED) SHANGHAI SUPER GLOVES CO., LTD.


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