510(k) K083681
K083681 is an FDA 510(k) premarket notification submitted by Bioland Technology, Ltd. for the device "BIOLAND BLOOD PRESSURE MONITOR". The FDA issued a decision of Substantially Equivalent on Jan 16, 2009. The device falls under product code DXN (System, Measurement, Blood-Pressure, Non-Invasive), a Class II device regulated under 21 CFR 870.1130. Bioland Technology, Ltd. has 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jan 16, 2009
- Date Received
- Dec 12, 2008
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
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)