Konica Minolta Sensing, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K053419 | KONICA MINOLTA PULSOX-300, 300I | DQA | 2006-05-11 | View |
| 510(k) | K021469 | MINOLTA PULSOX-2 | DQA | 2003-02-12 | View |
| 510(k) | K010413 | MINOLTA PULSOX-3SI, PULSOX-3IA, PULSOX-3LI | DQA | 2001-08-02 | View |
No matching devices.
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