Terumo Medical Corp.
FDA 510(k) & PMA Approved Devices — 143 products
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Total Devices143
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K111606 | PINNACLE PRECISION ACCESS SYSTEM | DYB | 2011-10-03 | View |
| 510(k) | K111556 | GLIDECROSS SUPPORT CATHETER | DQY | 2011-07-29 | View |
| 510(k) | K110540 | TERUMO SUPPORT CATHETER | DQY | 2011-05-13 | View |
| 510(k) | K102008 | GLIDESHEATH | DYB | 2010-07-21 | View |
| 510(k) | K091329 | PINNACLE DESTINATION PERIPHERAL GUIDING SHEATH | DYB | 2009-05-29 | View |
| 510(k) | K082997 | TERUMO HYBRIA CLOSED SYSTEM SAFETY I.V. CATHETER | FOZ | 2009-04-15 | View |
| 510(k) | K090040 | RADIFOCUS GLIDECATH (OR RADIFOCUS GLIDECATH XP) | DQO | 2009-02-06 | View |
| 510(k) | K082847 | PINNACLE ROII INTRODUCER SHEATH | DYB | 2008-10-29 | View |
| 510(k) | K082519 | FINECROSS MG CORONARY MICRO-GUIDE CATHETER | KRA | 2008-09-26 | View |
| 510(k) | K082736 | RADIFOCUS OPTITORQUE ANGIOGRAPHIC CATHETER | DQO | 2008-09-24 | View |
| 510(k) | K082644 | GLIDESHEATH | DYB | 2008-09-18 | View |
| 510(k) | K082362 | SURSHIELD SAFETY I.V. CATHETER | FOZ | 2008-09-17 | View |
| 510(k) | K081045 | DESTINATION RENAL GUIDING SHEATH | DYB | 2008-05-28 | View |
| 510(k) | K081046 | PINNACLE DESTINATION PERIPHERAL GUIDING SHEATH | DYB | 2008-05-21 | View |
| 510(k) | K080563 | RUNTHROUGH NS EXTENSION WIRE | DQX | 2008-03-20 | View |
| 510(k) | K080415 | DEVICE MODIFICATION TO PINNACLE DESTINATION PERIPHERAL GUIDING SHEATH | DYB | 2008-03-07 | View |
| 510(k) | K071630 | TERUMO 31G THINPRO INSULIN SYRINGE | FMF | 2007-07-11 | View |
| 510(k) | K063695 | RUNTHROUGH NS | DQX | 2007-04-27 | View |
| 510(k) | K070423 | TR BAND | DXC | 2007-03-28 | View |
| 510(k) | K063372 | RADIFOCUS GLIDEWIRE ADVANTAGE | DQX | 2007-01-19 | View |
No matching devices.
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