Clearance Summary
CHAMPION, 3000 REBEL received FDA 510(k) clearance under submission number K953427, sponsored by Kuschall of America. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1995-07-31.
- Submission: K953427
- Applicant / Sponsor: Kuschall of America
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.3850
- Decision date: 1995-07-31
Classification & Regulation
This clearance is catalogued under FDA product code IOR and 21 CFR 890.3850, within the Physical Medicine review panel as a Class I device.