Device Classification Name |
System, Measurement, Blood-Pressure, Non-Invasive
More FDA Info for this Device |
510(K) Number |
K032695 |
Device Name |
System, Measurement, Blood-Pressure, Non-Invasive |
Applicant |
HEALTH & LIFE CO., LTD.
9F, NO.186, JIAN YI ROAD
CHUNG HO CITY, TAIPEI 235 TW
Other 510(k) Applications for this Company
|
Contact |
PAUL HUNG
Other 510(k) Applications for this Contact |
Regulation Number |
870.1130
More FDA Info for this Regulation Number |
Classification Product Code |
DXN
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
09/02/2003 |
Decision Date |
10/02/2003 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
CV - Cardiovascular |
Review Advisory Committee |
CV - Cardiovascular |
Statement / Summary / Purged Status |
Statement |
Type |
Special |
Reviewed By Third Party |
N |
Expedited Review |
|