Mediana Co., Ltd. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Mediana Co., Ltd. has 10 FDA 510(k) cleared medical devices. Based in Flintville, US.
Historical record: 10 cleared submissions from 2005 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Mediana Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Mediana Co., Ltd.
10 devices
Cleared
Oct 09, 2020
V20, V20a, AVSM3 SNF
Cardiovascular
228d
Cleared
Dec 15, 2017
V10
Cardiovascular
301d
Cleared
Feb 24, 2017
DT-100
General Hospital
381d
Cleared
Aug 25, 2016
V10
Cardiovascular
343d
Cleared
Nov 09, 2011
PATIENT MONITOR
Cardiovascular
103d
Cleared
Nov 08, 2011
FM20
Obstetrics & Gynecology
250d
Cleared
Jun 24, 2011
F10
Obstetrics & Gynecology
113d
Cleared
Feb 09, 2011
PULSE OXIMETER MODEL P10
Anesthesiology
379d
Cleared
Jun 08, 2010
LUCON M-SERIES PATIENT MONITOR, MODELS M20 AND M30
Cardiovascular
134d
Cleared
Jul 28, 2005
VITAL SIGNS MONITOR
Cardiovascular
63d