Cardiopulmonary Corp.
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) | K130208 | BERNOULLI ENTERPRISE SOFTWARE | MHX | 2013-12-20 | View |
| 510(k) | K091461 | BERNOULLI MANAGEMENT SYSTEM, OXINET III AND LIFEGARD VUE | MOD | 2009-08-14 | View |
| 510(k) | K061932 | BERNOULLI MANAGEMENT SYSTEM (MS) SOFTWARE | MSX | 2006-09-14 | View |
| 510(k) | K051283 | MODIFICATION TO BERNOULLI VENTILATOR MANAGEMENT SYSTEM SOFTWARE | MSX | 2005-06-23 | View |
| 510(k) | K020018 | MODIFICATION TO BERNOULLI VENTILATOR MANAGEMENT SYSTEM SOFTWARE | MSX | 2002-02-21 | View |
| 510(k) | K011861 | BERNOULLI VENTILATOR MANAGEMENT SYSTEM | MOD | 2001-11-06 | View |
| 510(k) | K990429 | MODIFICATION OF VENTURI VENTILATOR | CBK | 1999-02-24 | View |
| 510(k) | K982174 | VENTURI VENTILATOR | CBK | 1998-06-24 | View |
| 510(k) | K943412 | VENTURI VENTILATOR | CBK | 1995-10-16 | View |
No matching devices.
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