Medical Device Manufacturer · CH , Thun, Bern

Meridian AG - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2002
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Meridian AG General & Plastic Surgery ✕
2 devices
1-2 of 2
Cleared May 19, 2017
MICRORUPTOR 6
K160677 · GEX
General & Plastic Surgery · 435d
Cleared Feb 14, 2012
LASER INDIRECT OPHTHALMOSCOPE 500(LIO-500)
K113390 · GEX
General & Plastic Surgery · 90d
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