510(k) K030221
K030221 is an FDA 510(k) premarket notification submitted by Mytech Technology Co., Ltd. for the device "MYTECH / HAPPY LIFE BLOOD PRESSURE MONITOR". The FDA issued a decision of Substantially Equivalent on Jul 25, 2003. The device falls under product code DXN (System, Measurement, Blood-Pressure, Non-Invasive), a Class II device regulated under 21 CFR 870.1130. Mytech Technology Co., Ltd. has 3 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jul 25, 2003
- Date Received
- Jan 21, 2003
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- System, Measurement, Blood-Pressure, Non-Invasive
- Device Class
- Class II
- Regulation Number
- 870.1130
- Review Panel
- CV
- Submission Type
- 510(k)