Lumitex, 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) | K120820 | GIRAFFE BLUE SPOT PT LITE | LBI | 2012-06-08 | View |
| 510(k) | K053568 | BILISOFT PHOTOTHERAPY SYSTEM | LBI | 2006-04-17 | View |
| 510(k) | K912747 | LULMITEX NEONATAL TRANSILLUMINATOR | HJN | 1991-12-24 | View |
No matching devices.
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