Cardio Systems, Inc.
FDA 510(k) & PMA Approved Devices — 9 products
Advertisement
Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K131092 | STEALTH 360 ORBITAL PAD SYSTEM | MCW | 2013-06-24 | View |
| 510(k) | K081944 | MODIFICATION TO DIAMONDBACK 360 DEGREE ORBITAL ATHERECTOMY SYSTEM | MCW | 2008-08-14 | View |
| 510(k) | K972022 | ZAK-2000 | FNM | 1998-01-22 | View |
| 510(k) | K934689 | LOW AIR LOSS MATTRESS, MODIFICATION | INX | 1994-02-02 | View |
| 510(k) | K921500 | CENTRI-SAFE(TM) VALVE | MJJ | 1992-09-15 | View |
| 510(k) | K882177 | ADD-ON TO CRITICAL PATIENT CARE BED | IOQ | 1988-12-01 | View |
| 510(k) | K852736 | BAYLOR RAPID AUTOTRANSFUSION SYSTEM | CAC | 1985-09-18 | View |
| 510(k) | K792152 | CARDIOPLEGIA SOLUTION ADMIN. SET | DWF | 1979-11-13 | View |
| 510(k) | K792151 | OXYGENATOR GAS LINE FILTER | KRI | 1979-11-13 | View |
No matching devices.
Advertisement