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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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