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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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