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FDA 510(k) Applications Submitted by SHANDONG PERFECT PLASTIC CO., LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K042213
08/16/2004
PRE-POWDERED NON-STERILE VINYL EXAMINATION GLOVES
SHANDONG PERFECT PLASTIC CO., LTD.
K042214
08/16/2004
POWDER-FREE NON-STERILE VINYL EXAMINATION GLOVES
SHANDONG PERFECT PLASTIC CO., LTD.
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