Meridian AG

Meridian AG holds 6 FDA 510(k) medical device clearances, first cleared 2002, most recent 2024.

Top product codes for Meridian AG

Recent clearances by Meridian AG

K232417 — MR Q; MR Q SUPINE; MR Q SLTCode HQF·2024-01-25
K231011 — Merilas 532 shortpulse, Merilas 577 shortpulse, Merilas 810 shortpulseCode HQF·2023-09-12
K160677 — MICRORUPTOR 6Code GEX·2017-05-19
K113390 — LASER INDIRECT OPHTHALMOSCOPE 500(LIO-500)Code GEX·2012-02-14
K072823 — MERILAS 532ACode HQF·2007-12-14
K023045 — MICRORUPTER VCode LXS·2002-09-26

Data sourced from openFDA. This site is unofficial and independent of the FDA.