MYTECH / HAPPY LIFE BLOOD PRESSURE MONITOR


Device Classification Name

system, measurement, blood-pressure, non-invasive

510(k) Number K030221
Device Name MYTECH / HAPPY LIFE BLOOD PRESSURE MONITOR
Original Applicant
MYTECH TECHNOLOGY CO., LTD.
no. 58, fu-chiun st.
hsin-chu city, 

TW

Original Contact jen ke-min
Regulation Number 870.1130
Classification Product Code
DXN  
Date Received 01/21/2003
Decision Date 07/25/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

statement

statement

Type Traditional
Reviewed by Third Party No

Combination Product

No