Jawon Medical Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K140762AUTOMATIC BLOOD PRESSURE MONITORJuly 2, 2015
K140045BODY COMPOSITION ANALYZERFebruary 18, 2015
K092432AUTOMOATIC BLOOD PRESSURE MONITOR, MODELS: EASY X 800 AND 900 (R/L)October 9, 2009
K092431BODY COMPOSITION ANALYZER, MODEL: IOI 353October 8, 2009
K072325BODY COMPOSITION ANALYZER, EASYBODY 202, 203, 205November 30, 2007
K071884BODY COMPOSITION ANALYZER, MODELS: X-SCAN PLUS II, GAIA 359 PLUS, PLUSAVIS 333, XBIA 500, XBIA 900August 9, 2007
K062462NON-INVASIVE BLOOD PRESSURE MONITOR, MODELS FT-500R/L AND FT-700R/LSeptember 29, 2006
K053556BODY COMPOSITION ANALYZER, MODELS ZEUS 9.9 AND VENUS 5.5August 31, 2006
K013876INFRARED EAR THERMOMETER, MODEL DX-707March 4, 2002
K002722DIGITAL BLOOD PRESSURE MONITOR, MODELS HD-503 AND HD-505September 11, 2000
K000675MANUAL DIGITAL BLOOD PRESSURE MONITOR, MODEL HD-502March 14, 2000
K991688WRIST TYPE DIGITAL BLOOD PRESSURE MONITOR, MODEL HD-303SJune 1, 1999
K983855FUZZY TYPE DIGITAL BLOOD PRESSURE MONITOR, MODEL #'S HD-1000S & HD-2000FNovember 17, 1998