Clearance Summary
THE CAROLINA ROCKER received FDA 510(k) clearance under submission number K900839, sponsored by Artec Environmental Monitoring Division. 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 1990-04-18.
- Submission: K900839
- Applicant / Sponsor: Artec Environmental Monitoring Division
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.3920
- Decision date: 1990-04-18
Classification & Regulation
This clearance is catalogued under FDA product code KNN and 21 CFR 890.3920, within the Physical Medicine review panel as a Class I device.