FDA 510(k) Applications Submitted by Ellex Medical Pty. Ltd.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K021550 |
05/13/2002 |
LUMENIS SELECTA DUET |
Ellex Medical Pty. Ltd. |
| K992824 |
08/23/1999 |
LASEREX ND:YAG OPHTHALMIC LASER (LQ2106), ALCON ND:YAG OPHTHALMIC LASER (3000LE), LASEREX ND:YAG OPHTHALMIC LASER, MODEL |
Ellex Medical Pty. Ltd. |
| K003955 |
12/21/2000 |
LASEREX INTEGRE, MODEL LP2532 |
Ellex Medical Pty. Ltd. |
| K972514 |
07/07/1997 |
LASEREX LP1532 PHOTOCOAGULATOR |
Ellex Medical Pty. Ltd. |
| K080423 |
02/15/2008 |
INTEGRE, MODEL LP581 |
Ellex Medical Pty. Ltd. |
| K081565 |
06/04/2008 |
INTEGRE PRO, MODEL L2RY |
Ellex Medical Pty. Ltd. |
| K041598 |
06/14/2004 |
LASEREX, MODEL LP4532 |
Ellex Medical Pty. Ltd. |
| K122202 |
07/25/2012 |
ELLEX 2RT |
Ellex Medical Pty. Ltd. |
| K142398 |
08/27/2014 |
Integre Pro Scan Green, Integre Pro Scan Yellow, Integre Pro Scan Red-Green, Integre Pro Scan Red-Yellow |
Ellex Medical Pty. Ltd. |
| K052777 |
10/03/2005 |
LASEREX DUO FAMILY OF DUAL WAVELENGTH OPHTHALMIC LASERS INCLUDING MODELS INTEGRE DUO LP1RG-S, LP1RG-D |
Ellex Medical Pty. Ltd. |
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