Carefusion 2200, Inc.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K210324 | V. Mueller Cosgrove Flex Clamps, Model Number-CV1033, CV1061, CV1133, CV1161, CV1186 | DXC | 2021-03-04 | View |
| 510(k) | K163615 | Snowden-Pencer MicroLap 3mm Laparoscopic Instruments | GEI | 2017-05-04 | View |
| 510(k) | K162432 | Multi-Link X2 ECG Cable and Lead Wire System | DSA | 2017-01-18 | View |
| 510(k) | K160764 | AirLife Autofill Humidification Chamber | BTT | 2016-08-25 | View |
| 510(k) | K153554 | Genesis Low Temperature Reusable Rigid Container System | KCT | 2016-03-21 | View |
| 510(k) | K151036 | Snowden-Pencer Ergonomic Take-Apart In-Line and Pistol Grip Laparoscopic Instruments | GCJ | 2016-02-01 | View |
| 510(k) | K113407 | SNOWDEN PENCER LAPAROSCOPIC ERGONOMIC REPOSABLE SCISSORS | GEI | 2012-09-07 | View |
| 510(k) | K112535 | GENESIS REUSABLE RIGID CONTAINER SYSTEM | KCT | 2012-04-27 | View |
| 510(k) | K110257 | DIAMOND-FLEX(R) GRASPERS | GCJ | 2011-05-06 | View |
No matching devices.
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