510(k) K123130
K123130 is an FDA 510(k) premarket notification submitted by Taiwan Scientific Corporation for the device "ANSWATCH WRIST MONITOR MODEL TS-0411". The FDA issued a decision of Substantially Equivalent on Sep 17, 2013. The device falls under product code DXN (System, Measurement, Blood-Pressure, Non-Invasive), a Class II device regulated under 21 CFR 870.1130. Taiwan Scientific Corporation has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Sep 17, 2013
- Date Received
- Oct 4, 2012
- 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)