Boston Scientific/Medi-Tech is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Boston Scientific/Medi-Tech - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Boston Scientific/Medi-Tech has 5 FDA 510(k) cleared medical devices. Based in Natick,, US.
Historical record: 5 cleared submissions from 2001 to 2002. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Boston Scientific/Medi-Tech Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Boston Scientific/Medi-Tech
5 devices
Cleared
Dec 20, 2002
FLEXIMA BILIARY CATHETER
Gastroenterology & Urology
30d
Cleared
Jan 29, 2002
MODIFICATION TO RENEGADE FIBER BRAIDED MICROCATHETER
Cardiovascular
26d
Cleared
Oct 03, 2001
MODIFICATION TO VAXCEL DIALYSIS CATHETER
Gastroenterology & Urology
29d
Cleared
Oct 02, 2001
HEMASHIELD GOLD WOVEN DOUBLE VELOUR VASCULAR GRAFT - BRANCH GRAFT
Cardiovascular
28d
Cleared
Sep 07, 2001
IMAGER II ANGIOGRAPHIC CATHETER
Cardiovascular
100d