Medical Device Manufacturer · KR , Songpa-Gu, Seoul

Meridian Co., Ltd. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2000
7
Total
7
Cleared
0
Denied

FDA 510(k) Regulatory Record - Meridian Co., Ltd. Neurology ✕

3 devices
1-3 of 3
Cleared Aug 29, 2002
ABR-2000
K020360 · GZO
Neurology · 206d
Cleared Jun 19, 2001
MERIDIAN-PORTABLE
K010897 · GZO
Neurology · 85d
Cleared Nov 03, 2000
MERIDIAN-II AND MERDIAN-PLUS
K001347 · GZO
Neurology · 189d
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