Iridex Corp
FDA 510(k) & PMA Approved Devices — 13 products
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Total Devices13
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K121475 | TXCELL SCANNING LASER DELIVERY SYSTEM | GEX | 2012-11-28 | View |
| 510(k) | K071687 | FAMILI OF IRIDEX IQ LASER SYSTEMS | GEX | 2008-08-07 | View |
| 510(k) | K062074 | IRIDEX WIRELESS FOOTSWITCH | HQF | 2006-11-14 | View |
| 510(k) | K062369 | IRIDEX OCULIGHT TX | GEX | 2006-11-08 | View |
| 510(k) | K060905 | IRIDEX OTOPROBE LONG AND SHORT ANGLES, P/N 14310-1 AND 14320-1 | GEX | 2006-05-31 | View |
| 510(k) | K050562 | OCULIGHT GL/GLX | GEX | 2005-04-14 | View |
| 510(k) | K040209 | IRIS MEDICAL IQ 810 PHOTOCOAGULATOR | HQF | 2004-09-20 | View |
| 510(k) | K031665 | IRIS MEDICAL OCULIGHT GL/GLX LASER SYSTEMS | HQF | 2003-08-27 | View |
| 510(k) | K022228 | FAMILY OF IRIS MEDICAL ENDOPROBE HANDPIECES | GEX | 2002-10-08 | View |
| 510(k) | K020849 | APEX 800 LASER SYSTEM, MODEL APEX 800 | GEX | 2002-05-20 | View |
| 510(k) | K020374 | OCULIGHT SL/SLX | HQF | 2002-05-03 | View |
| 510(k) | K992298 | IRIDERM, MODEL APEX 800 | GEX | 1999-12-09 | View |
| 510(k) | K982031 | OCULIGHT GL WITH THE DERMATOLOGY HANDPIECE | GEX | 1998-09-08 | View |
No matching devices.
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