510(k) K033514
K033514 is an FDA 510(k) premarket notification submitted by Charnwood Dynamics , Ltd. for the device "CODA CX1 MOTION ANALYSIS SYSTEM". The FDA issued a decision of Substantially Equivalent on Jan 6, 2004. The device falls under product code LXJ (Interactive Rehabilitation Exercise Devices), a Class II device regulated under 21 CFR 890.5360.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jan 6, 2004
- Date Received
- Nov 6, 2003
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Interactive Rehabilitation Exercise Devices
- Device Class
- Class II
- Regulation Number
- 890.5360
- Review Panel
- PM
- Submission Type
- 510(k)