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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