510(k) K123882
K123882 is an FDA 510(k) premarket notification submitted by Ageless Health Industrial for the device "AGE AUTOMATIC UPPER ARM BLOOD PRESSURE MONITOR". The FDA issued a decision of Substantially Equivalent on Aug 14, 2013. The device falls under product code DXN (System, Measurement, Blood-Pressure, Non-Invasive), a Class II device regulated under 21 CFR 870.1130.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Aug 14, 2013
- Date Received
- Dec 17, 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)