I.L. Med, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K905511 | CODMAN NEUROLASE LASER SYSTEM/MODIFICATION | GEX | 1991-03-05 | View |
| 510(k) | K883642 | CODMAN NEUROLASE LASER SYSTEM | GEX | 1988-10-20 | View |
No matching devices.
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