Lasersight Technologies, 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) | K001144 | ULTRAEDGE KERATOME BLADE, MODEL 374803 - ACS | HNO | 2000-05-05 | View |
| 510(k) | K990227 | ULTRASHAPER KERATOME | HNO | 2000-01-31 | View |
| 510(k) | K974004 | AUTOMATED DISPOSABLE KERATOME (ADK) | HNO | 1998-01-08 | View |
No matching devices.
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