510(k) K032492
K032492 is an FDA 510(k) premarket notification submitted by K-Jump Health Co., Ltd. for the device "BLOOD PRESSURE MONITOR, MODEL KP-7000". The FDA issued a decision of Substantially Equivalent on September 9, 2003. The device falls under product code DXN (System, Measurement, Blood-Pressure, Non-Invasive), a Class II device regulated under 21 CFR 870.1130. K-Jump Health Co., Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 9, 2003
- Date Received
- August 12, 2003
- Clearance Type
- Special
- 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