FDA 510(k) Applications Submitted by STEVE CHANG
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K073058 |
10/30/2007 |
RESCUE INTERNAL IMPLANT SYSTEM |
MEGAGEN CO., LTD. |
K073070 |
10/30/2007 |
DIO BIOTITE-H IMPLANT SYSTEM |
DIO DEPARTMENT DSI, INC. |
K070086 |
01/09/2007 |
SENSACARE MODEL SAA-102 ARM TYPE DIGITAL BLOOD PRESSURE MONITOR |
SENSACARE LTD. |
K050680 |
03/16/2005 |
BLOOD PRESSURE MONITOR WITH SPECTRUM/P2, X2, A2, AND K7 |
OSTAR MEDITECH CORP. |
K081590 |
06/06/2008 |
YA HORNG ARM TYPE DIGITAL BLOOD PRESSURE MONITOR, MODELS BP-600, BP-600R, BP-600U, BP-600B, BP-600RB, BP-600UB, BP-600J |
YA HORNG ELECTRONIC CO., LTD. |
K061935 |
07/10/2006 |
SENSACARE SAW-102 WRIST DIGITAL BLOOD PRESSURE MONITOR |
SENSACARE LTD. |
K112269 |
08/08/2011 |
OSTAR USB BLOOD PRESSURE MONITOR WITH SPECTRUM / P200 FOR UPPER ARM, AND M100 FOR WRIST TYPE |
OSTAR MEDITECH CORP. |
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