510(k) K123669
K123669 is an FDA 510(k) premarket notification submitted by Zhongshan Transtek Electronics Co., Ltd. for the device "TRANSTEK WRIST BLOOD PRESSURE MONITOR". The FDA issued a decision of Substantially Equivalent on December 21, 2012. The device falls under product code DXN (System, Measurement, Blood-Pressure, Non-Invasive), a Class II device regulated under 21 CFR 870.1130. Zhongshan Transtek Electronics Co., Ltd. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 21, 2012
- Date Received
- November 29, 2012
- Clearance Type
- Special
- 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