Clinicon Corp.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K121580 | SURELASE CO2 LASER SYSTEM | GEX | 2012-09-25 | View |
| 510(k) | K063698 | CO2 LASER SYSTEM, MODEL C-LAS | GEX | 2007-03-02 | View |
| 510(k) | K014236 | CLINICON WAVEGUIDE PLATFORM WITH INTERCONNECT FOR LUXAR ACCESSORIES | GEX | 2002-03-26 | View |
| 510(k) | K014048 | CLINICON UNIVERSAL WAVEGUIDE HANDPIECE AND FIBER TIPS | GEX | 2002-02-11 | View |
| 510(k) | K992472 | SUREGUIDE CO2 LASER BEAM DELIVERY SYSTEM | GEX | 1999-09-08 | View |
| 510(k) | K983463 | SURECAUT DIAMOND LASER KNIFE | GEX | 1998-12-11 | View |
| 510(k) | K970143 | C4 | GEX | 1997-10-29 | View |
| 510(k) | K964831 | SURESCAN | GEX | 1997-08-08 | View |
| 510(k) | K962242 | SURESCAN | GEX | 1996-09-03 | View |
No matching devices.
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