Qrs Diagnostic, LLC
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K083749 | CARDIOVIEW32 REVIEW MODULE | LOS | 2009-03-10 | View |
| 510(k) | K073630 | MODIFICATION TO: BPCARD, MODEL Z-7000-0700 | DXN | 2008-01-11 | View |
| 510(k) | K031964 | BPCARD | DXN | 2003-09-05 | View |
| 510(k) | K030535 | EKGCARD SYSTEM | DPS | 2003-06-11 | View |
| 510(k) | K001278 | SENSAIRE DIAGNOSTIC SPIROMETER | BZG | 2000-11-29 | View |
| 510(k) | K001995 | SPIROXCARD DIAGNOSTIC SPIROMETER AND PULSE OXIMETER | DQA | 2000-09-08 | View |
| 510(k) | K973138 | SPIROCARD | BZG | 1998-10-28 | View |
No matching devices.
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