Allmed Systems, Inc.
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) | K110941 | REVOLIX JR 30, REVOLIX JR 50, REVOLIX JR 160, REVOLIX FR 200 | GEX | 2013-02-19 | View |
| 510(k) | K070924 | FLEXGUARD | GEX | 2007-06-21 | View |
| 510(k) | K070466 | REVOLIX DUO LASER SYSTEM | GEX | 2007-04-17 | View |
| 510(k) | K070476 | REVOLIX 120 | GEX | 2007-03-26 | View |
| 510(k) | K051167 | REVOLIX AND REVOLIX JR | GEX | 2005-06-01 | View |
| 510(k) | K033437 | SPHINX LASER SYSTEMS | GEX | 2004-01-20 | View |
| 510(k) | K033423 | REVOLIX LASER SYSTEMS | GEX | 2004-01-15 | View |
No matching devices.
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