Litecure, 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) | K173067 | LightForce LTS Model 1000, 1500, 2500, and 4000 | GEX | 2018-02-22 | View |
| 510(k) | K123014 | LITECURE THERAPY SYSTEM MODEL LTS-1500 | PDZ | 2013-03-29 | View |
| 510(k) | K123031 | BWF-5 MEDICAL LASER SERIES | GEX | 2012-12-03 | View |
| 510(k) | K121487 | LITECURE THERAPY COMPACT | ILY | 2012-06-12 | View |
| 510(k) | K103511 | LITECURE THERAPY SYSTEM | ILY | 2011-01-25 | View |
| 510(k) | K093087 | BWF-5 MEDICAL LASER SERIES | GEX | 2010-05-12 | View |
| 510(k) | K070400 | LC THERAPY, MODEL LCT-1000 | ILY | 2007-02-28 | View |
No matching devices.
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