510(k) K911965
K911965 is an FDA 510(k) premarket notification submitted by Citizen Watch Co., Ltd. for the device "ELECTRONIC DIGITAL BLOOD PRESSURE/PULSE MONITOR". The FDA issued a decision of Substantially Equivalent on Oct 28, 1991. The device falls under product code DXN (System, Measurement, Blood-Pressure, Non-Invasive), a Class II device regulated under 21 CFR 870.1130. Citizen Watch Co., Ltd. has 7 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 28, 1991
- Date Received
- May 2, 1991
- 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)