Bipore, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bipore, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Bipore, Inc. has 10 FDA 510(k) cleared cardiovascular devices. Based in Demarest, US.
Historical record: 10 cleared submissions from 1985 to 2008.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bipore, Inc.
10 devices
Cleared
Apr 01, 2008
BIPORE ACCUFLEX PERCUTANEOUS SHEATH INTRODUCER
Cardiovascular
117d
Cleared
Jan 16, 2008
BIPORE BALLOON DILATION CATHETER
Cardiovascular
51d
Cleared
Dec 07, 2005
BIPORE ACCUFLEX PERCUTANEOUS SHEATH INTRODUCER
Cardiovascular
188d
Cleared
Jul 09, 2004
BIOPORE BALLOON DILATION CATHETER
Cardiovascular
56d
Cleared
Feb 17, 1999
BIPORE BALLOON DILATATION CATHETER
Cardiovascular
124d
Cleared
Apr 01, 1998
BIPORE BALLOON DILATATION CATHETER
Cardiovascular
194d
Cleared
May 07, 1997
BIPORE ACCUFLEX PERCUTANEOUS SHEATH INTRODUCER
Cardiovascular
159d
Cleared
Sep 12, 1996
BIPORE BALLOON DILATATION CATHETER
Cardiovascular
115d
Cleared
Jul 22, 1986
O.2 MICRON INFECTION RESISTANT HYDROPHOBIC FILTER
Gastroenterology & Urology
55d
Cleared
Jan 16, 1985
BIPORE O.2 MICRON HYDROPHOBIC FILTER ASSEMBLY
General & Plastic Surgery
50d