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Bipore, Inc.

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K073434	BIPORE ACCUFLEX PERCUTANEOUS SHEATH INTRODUCER	DYB	2008-04-01	View
510(k)	K073318	BIPORE BALLOON DILATION CATHETER	LIT	2008-01-16	View
510(k)	K051513	BIPORE ACCUFLEX PERCUTANEOUS SHEATH INTRODUCER	DYB	2005-12-07	View
510(k)	K041293	BIOPORE BALLOON DILATION CATHETER	LIT	2004-07-09	View
510(k)	K983650	BIPORE BALLOON DILATATION CATHETER	LIT	1999-02-17	View
510(k)	K973563	BIPORE BALLOON DILATATION CATHETER	LIT	1998-04-01	View
510(k)	K964814	BIPORE ACCUFLEX PERCUTANEOUS SHEATH INTRODUCER	DYB	1997-05-07	View
510(k)	K961980	BIPORE BALLOON DILATATION CATHETER	LIT	1996-09-12	View
510(k)	K862015	O.2 MICRON INFECTION RESISTANT HYDROPHOBIC FILTER	FIB	1986-07-22	View
510(k)	K844625	BIPORE O.2 MICRON HYDROPHOBIC FILTER ASSEMBLY	KOZ	1985-01-16	View

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