Bipore, Inc.

10 FDA 510(k) medical device clearances.

Top product codes for Bipore, Inc.

LIT — Cardiovascular 5 devices
DYB — Cardiovascular 3 devices
FIB — Gastroenterology, Urology 1 device
KOZ — General, Plastic Surgery 1 device

Recent clearances by Bipore, Inc.

K073434 — BIPORE ACCUFLEX PERCUTANEOUS SHEATH INTRODUCER DYB · 2008-04-01
K073318 — BIPORE BALLOON DILATION CATHETER LIT · 2008-01-16
K051513 — BIPORE ACCUFLEX PERCUTANEOUS SHEATH INTRODUCER DYB · 2005-12-07
K041293 — BIOPORE BALLOON DILATION CATHETER LIT · 2004-07-09
K983650 — BIPORE BALLOON DILATATION CATHETER LIT · 1999-02-17
K973563 — BIPORE BALLOON DILATATION CATHETER LIT · 1998-04-01
K964814 — BIPORE ACCUFLEX PERCUTANEOUS SHEATH INTRODUCER DYB · 1997-05-07
K961980 — BIPORE BALLOON DILATATION CATHETER LIT · 1996-09-12
K862015 — O.2 MICRON INFECTION RESISTANT HYDROPHOBIC FILTER FIB · 1986-07-22
K844625 — BIPORE O.2 MICRON HYDROPHOBIC FILTER ASSEMBLY KOZ · 1985-01-16

Data sourced from openFDA. This site is unofficial and independent of the FDA.