Astralite Corp.
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) | K023004 | LFRE INDIRECT LARYNGOSCOPE | EOB | 2003-01-28 | View |
| 510(k) | K893813 | FLOOR STANDING, OPERATING AND EXAMINING LIGHT | FSS | 1989-07-14 | View |
No matching devices.
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