Philips Digital Mammography Sweden AB
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) | K130704 | MICRODOSE SI | MUE | 2013-12-13 | View |
| 510(k) | K123995 | MICRODOSE SI | MUE | 2013-02-01 | View |
| 510(k) | K120255 | PHILIPS MICRODOSE | MUE | 2012-04-19 | View |
No matching devices.
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