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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