Mediana Co., Ltd. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
FDA 510(k) cleared devices by Mediana Co., Ltd. Cardiovascular ✕
6 devices
Cleared
Oct 09, 2020
V20, V20a, AVSM3 SNF
Cardiovascular
228d
Cleared
Dec 15, 2017
V10
Cardiovascular
301d
Cleared
Aug 25, 2016
V10
Cardiovascular
343d
Cleared
Nov 09, 2011
PATIENT MONITOR
Cardiovascular
103d
Cleared
Jun 08, 2010
LUCON M-SERIES PATIENT MONITOR, MODELS M20 AND M30
Cardiovascular
134d
Cleared
Jul 28, 2005
VITAL SIGNS MONITOR
Cardiovascular
63d