FDA 510(k) Applications Submitted by MERIDIAN AG
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K231011 | 04/10/2023 | Merilas 532 shortpulse, Merilas 577 shortpulse, Merilas 810 shortpulse | Meridian AG |
| K160677 | 03/10/2016 | MICRORUPTOR 6 | MERIDIAN AG |
| K072823 | 10/02/2007 | MERILAS 532A | MERIDIAN AG |
| K113390 | 11/16/2011 | LASER INDIRECT OPHTHALMOSCOPE 500(LIO-500) | MERIDIAN AG |
| K023045 | 09/12/2002 | MICRORUPTER V | MERIDIAN AG |
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