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Mediana Co., Ltd.

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K200434	V20, V20a, AVSM3 SNF	DXN	2020-10-09	View
510(k)	K170497	V10	DXN	2017-12-15	View
510(k)	K160358	DT-100	FLL	2017-02-24	View
510(k)	K152659	V10	DXN	2016-08-25	View
510(k)	K112190	PATIENT MONITOR	MHX	2011-11-09	View
510(k)	K110612	FM20	HGM	2011-11-08	View
510(k)	K110630	F10	KNG	2011-06-24	View
510(k)	K100225	PULSE OXIMETER MODEL P10	DQA	2011-02-09	View
510(k)	K100217	LUCON M-SERIES PATIENT MONITOR, MODELS M20 AND M30	MHX	2010-06-08	View
510(k)	K051375	VITAL SIGNS MONITOR	DXN	2005-07-28	View

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