FDA 510(k) Applications Submitted by FORMOSA GLOVE INDUSTRIAL CO., LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K992588 08/02/1999 BLUE NITRILE PATIENT EXAMINATION GLOVES, POWDER-FREE FORMOSA GLOVE INDUSTRIAL CO., LTD.
K014284 12/27/2001 NITRILE PATIENT EXAMINATION GLOVES, POWDER-FREE AND YELLOWISH WHITE FORMOSA GLOVE INDUSTRIAL CO., LTD.
K014285 12/27/2001 NITRILE PATIENT EXAMINATION GLOVES, POWDER-FREE, PURPLE FORMOSA GLOVE INDUSTRIAL CO., LTD.


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