510(k) K081852
K081852 is an FDA 510(k) premarket notification submitted by Truly Instrument Limited for the device "TRULY AUTOMATIC BLOOD PRESSURE MONITOR, MODEL DB11". The FDA issued a decision of Substantially Equivalent on Dec 12, 2008. The device falls under product code DXN (System, Measurement, Blood-Pressure, Non-Invasive), a Class II device regulated under 21 CFR 870.1130. Truly Instrument Limited has 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 12, 2008
- Date Received
- Jun 30, 2008
- 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)