510(k) K014204
K014204 is an FDA 510(k) premarket notification submitted by K-Jump Health Co., Ltd. for the device "ARM BLOOD PRESSURE MONITOR, MODELS KP-6821, KP-6822". The FDA issued a decision of Substantially Equivalent on March 5, 2002. 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
- March 5, 2002
- Date Received
- December 21, 2001
- 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