Iriderm Div.
FDA 510(k) & PMA Approved Devices — 10 products
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Total Devices10
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K964074 | DIOLITE 532 | GEX | 1997-04-01 | View |
| 510(k) | K960971 | OCULIGHT GL | HQF | 1996-08-28 | View |
| 510(k) | K960522 | DIOPEXY PROBE | HQF | 1996-07-19 | View |
| 510(k) | K915236 | IRIS G-PROBE | GEX | 1994-07-28 | View |
| 510(k) | K933211 | D'AMICO\PEYMAN FLUTED ENDOPROBE | GEX | 1994-04-19 | View |
| 510(k) | K922663 | IRIS OCULIGHT SL | GEX | 1992-08-11 | View |
| 510(k) | K913430 | IRIS OCULIGHT(R) SLX | GEX | 1991-11-15 | View |
| 510(k) | K912918 | IRIS OCULIGHT DIODE LASER ADDING SLIT LAMP ADAPTER | GEX | 1991-08-23 | View |
| 510(k) | K903288 | IRIS OCULIGHT SL DIODE LASER PHOTOCOAG/MODIFIED | GEX | 1990-09-24 | View |
| 510(k) | K894841 | IRIS OCULIGHT(TM) SL | GEX | 1989-10-05 | View |
No matching devices.
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