Medical Device Manufacturer · US , Elkton , MD

Terumo Medical Corp. - FDA 510(k) Cleared Devices

143 submissions · 143 cleared · Since 1980
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.

143 devices
1–12 of 143
PINNACLE PRECISION ACCESS SYSTEM
K111606 · DYB Introducer, Catheter · Cardiovascular
Oct 2011 116d
GLIDECROSS SUPPORT CATHETER
K111556 · DQY Catheter, Percutaneous · Cardiovascular
Jul 2011 53d
TERUMO SUPPORT CATHETER
K110540 · DQY Catheter, Percutaneous · Cardiovascular
May 2011 77d
GLIDESHEATH
K102008 · DYB Introducer, Catheter · Cardiovascular
Jul 2010 5d
PINNACLE DESTINATION PERIPHERAL GUIDING SHEATH
K091329 · DYB Introducer, Catheter · Cardiovascular
May 2009 24d
TERUMO HYBRIA CLOSED SYSTEM SAFETY I.V. CATHETER
K082997 · FOZ Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days · General Hospital
Apr 2009 189d
RADIFOCUS GLIDECATH (OR RADIFOCUS GLIDECATH XP)
K090040 · DQO Catheter, Intravascular, Diagnostic · Cardiovascular
Feb 2009 31d
PINNACLE ROII INTRODUCER SHEATH
K082847 · DYB Introducer, Catheter · Cardiovascular
Oct 2008 30d
FINECROSS MG CORONARY MICRO-GUIDE CATHETER
K082519 · KRA Catheter, Continuous Flush · Cardiovascular
Sep 2008 24d
RADIFOCUS OPTITORQUE ANGIOGRAPHIC CATHETER
K082736 · DQO Catheter, Intravascular, Diagnostic · Cardiovascular
Sep 2008 6d
GLIDESHEATH
K082644 · DYB Introducer, Catheter · Cardiovascular
Sep 2008 7d
SURSHIELD SAFETY I.V. CATHETER
K082362 · FOZ Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days · General Hospital
Sep 2008 30d

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