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Brightsway Holdings Sdn Bhd

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K992020	BRIGHTWAY BRAND LATEX SURGICAL GLOVES - STERILE (POWDERED)	KGO	1999-07-26	View
510(k)	K992021	BRIGHTWAY BRAND LATEX SURGICAL GLOVES - STERILE (POWDER FREE)	KGO	1999-07-23	View
510(k)	K991752	BRIGHTWAY BRAND BLUE COLOR LATEX EXAMINATION GLOVE, POWDERED CONTAINING 150 MLGM OR LESS OF WATER EXTRACTABLE PROTEIN PE	LYY	1999-06-23	View
510(k)	K991750	BRIGHTWAY BRAND BLUE COLOR LATEX EXAMINATION GLOVE, POWDER FREE CONTAINING 50 MLGM OR LESS OF WATER EXTRACTABLE PROTEIN	LYY	1999-06-23	View

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