Terumo Medical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Terumo Medical Corp. - FDA 510(k) Cleared Devices
Recent clearances: PINNACLE PRECISION ACCESS SYSTEM, GLIDECROSS SUPPORT CATHETER, TERUMO SUPPORT CATHETER
143
Total
143
Cleared
0
Denied
Terumo Medical Corp. has 143 FDA 510(k) cleared medical devices. Based in Elkton, US.
Historical record: 143 cleared submissions from 1980 to 2011. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Terumo Medical Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Terumo Medical Corp.
143 devices
Cleared
Oct 03, 2011
PINNACLE PRECISION ACCESS SYSTEM
Cardiovascular
116d
Cleared
Jul 29, 2011
GLIDECROSS SUPPORT CATHETER
Cardiovascular
53d
Cleared
May 13, 2011
TERUMO SUPPORT CATHETER
Cardiovascular
77d
Cleared
Jul 21, 2010
GLIDESHEATH
Cardiovascular
5d
Cleared
May 29, 2009
PINNACLE DESTINATION PERIPHERAL GUIDING SHEATH
Cardiovascular
24d
Cleared
Apr 15, 2009
TERUMO HYBRIA CLOSED SYSTEM SAFETY I.V. CATHETER
General Hospital
189d
Cleared
Feb 06, 2009
RADIFOCUS GLIDECATH (OR RADIFOCUS GLIDECATH XP)
Cardiovascular
31d
Cleared
Oct 29, 2008
PINNACLE ROII INTRODUCER SHEATH
Cardiovascular
30d
Cleared
Sep 26, 2008
FINECROSS MG CORONARY MICRO-GUIDE CATHETER
Cardiovascular
24d
Cleared
Sep 24, 2008
RADIFOCUS OPTITORQUE ANGIOGRAPHIC CATHETER
Cardiovascular
6d
Cleared
Sep 18, 2008
GLIDESHEATH
Cardiovascular
7d
Cleared
Sep 17, 2008
SURSHIELD SAFETY I.V. CATHETER
General Hospital
30d
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