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Meridian AG

FDA 510(k) & PMA Approved Devices — 6 products

Total Devices6
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K232417 MR Q; MR Q SUPINE; MR Q SLTHQF2024-01-25 View
510(k) K231011 Merilas 532 shortpulse, Merilas 577 shortpulse, Merilas 810 shortpulseHQF2023-09-12 View
510(k) K160677 MICRORUPTOR 6GEX2017-05-19 View
510(k) K113390 LASER INDIRECT OPHTHALMOSCOPE 500(LIO-500)GEX2012-02-14 View
510(k) K072823 MERILAS 532AHQF2007-12-14 View
510(k) K023045 MICRORUPTER VLXS2002-09-26 View
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