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FDA 510(k) Applications Submitted by SHIJIAZHUANG DILLY PLASTICS PRODUCTS CO., LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K992463
07/23/1999
SYNTHETIC POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
SHIJIAZHUANG DILLY PLASTICS PRODUCTS CO., LTD.
K992464
07/23/1999
SYNTHETIC POWDERED VINYL PATIENT EXAMINATION GLOVES
SHIJIAZHUANG DILLY PLASTICS PRODUCTS CO., LTD.
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