Device Classification Name |
System, Measurement, Blood-Pressure, Non-Invasive
More FDA Info for this Device |
510(K) Number |
K021252 |
Device Name |
System, Measurement, Blood-Pressure, Non-Invasive |
Applicant |
IDT TECHNOLOGY LIMITED
BLOCK C, 9/F., KAISER ESTATE,
PHASE 1, 41 MAN YUE STREET
HUNGHOM HK
Other 510(k) Applications for this Company
|
Contact |
LILY LI
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 |
04/19/2002 |
Decision Date |
06/17/2002 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
CV - Cardiovascular |
Review Advisory Committee |
CV - Cardiovascular |
Statement / Summary / Purged Status |
Statement |
Type |
Traditional |
Reviewed By Third Party |
N |
Expedited Review |
|