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Slim River Latex 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)	K933224	SLIMFLEX - POWDER FREE LATEX EXAMINATION GLOVES	LYY	1994-03-15	View
510(k)	K926440	POWDER-FREE EXAMINATION GLOVE	LYY	1993-10-05	View
510(k)	K905033	SLIMFLEX, PATIENT EXAMINATION GLOVES	LYY	1990-11-19	View
510(k)	K904936	PATIENT EXAMINATION GLOVES	LYY	1990-11-08	View

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