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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