FDA 510(k) Applications Submitted by Mediana Co., Ltd.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K110612 |
03/03/2011 |
FM20 |
MEDIANA CO., LTD. |
K110630 |
03/03/2011 |
F10 |
MEDIANA CO., LTD. |
K100217 |
01/25/2010 |
LUCON M-SERIES PATIENT MONITOR, MODELS M20 AND M30 |
MEDIANA CO., LTD. |
K100225 |
01/26/2010 |
PULSE OXIMETER MODEL P10 |
MEDIANA CO., LTD. |
K051375 |
05/26/2005 |
VITAL SIGNS MONITOR |
MEDIANA CO., LTD. |
K112190 |
07/29/2011 |
PATIENT MONITOR |
MEDIANA CO., LTD. |
K200434 |
02/24/2020 |
V20, V20a, AVSM3 SNF |
Mediana Co., Ltd. |
K170497 |
02/17/2017 |
V10 |
Mediana Co., Ltd. |
K160358 |
02/09/2016 |
DT-100 |
Mediana Co., Ltd. |
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