Invivo Corporation
FDA 510(k) & PMA Approved Devices — 26 products
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Total Devices26
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K213766 | dS FootAnkle 16Ch Coils for 1.5T and 3.0T, dS HiRes HandWrist 16Ch Coils for 1.5T and 3.0T, ds Small Extremity 16Ch Coils for 1.5T and 3.0T | MOS | 2021-12-23 | View |
| 510(k) | K212227 | Philips MR Patient Care Portal | MWI | 2021-09-30 | View |
| 510(k) | K212175 | DynaCAD | LLZ | 2021-08-02 | View |
| 510(k) | K193403 | UroNav System | LLZ | 2019-12-27 | View |
| 510(k) | K192200 | DynaCAD | LLZ | 2019-10-09 | View |
| 510(k) | K182561 | UroNav (Version 3.0) | LLZ | 2018-10-19 | View |
| 510(k) | K162177 | dS FootAnkle I6CH 1.5T Coil | MOS | 2016-09-14 | View |
| 510(k) | K162001 | 1.5T and 3.0T 16 CH GE Shoulder Coils | MOS | 2016-08-31 | View |
| 510(k) | K132359 | MRI PATIENT MONITORING SYSTEM | MWI | 2013-08-30 | View |
| 510(k) | K131382 | EXPRESSION MR200 MRI PATIENT MONITORING SYSTEM, EXPRESSION IP5 INFORMATION PORTAL | MWI | 2013-07-15 | View |
| 510(k) | K124061 | MRI PATIENT MONITORING SYSTEM (MODEL 865214) | MWI | 2013-02-22 | View |
| 510(k) | K122897 | SENSE HEAD 16 MODEL 800647, SENSE SPINE 16 MODEL 800646; SENSE TORSO 16 MODEL 800645 | MOS | 2012-12-21 | View |
| 510(k) | K122646 | DS BREAST 16CH I/T 1.5T DS BREAST 16CH I/T 3.0T | MOS | 2012-11-02 | View |
| 510(k) | K121424 | EXPRESSION INFORMATION PORTAL | MWI | 2012-06-13 | View |
| 510(k) | K120122 | SENSE MSK S 8CH 1.5T | MOS | 2012-02-10 | View |
| 510(k) | K111673 | 1.5T AND 3T 8-CHANNEL MEDIUM GENERAL PURPOSE FLEX COIL | MOS | 2011-12-23 | View |
| 510(k) | K103700 | ESSENTIAL MRI PATIENT MONITOR | DQA | 2011-03-15 | View |
| 510(k) | K103149 | 1.5T 16-CHANNEL HAND-WRIST COIL | MOS | 2011-01-03 | View |
| 510(k) | K093842 | 1.5T AND 3.0T GENERAL PURPOSE FLEX COILS | MOS | 2010-03-05 | View |
| 510(k) | K093284 | 1.0T 8-CHANNEL PANORAMA BREAST ARRAY COIL | MOS | 2010-02-01 | View |
No matching devices.
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