Clearance Summary
CAVITAT ULTRASOUND BONE DENSITOMETER (CAVITAT) received FDA 510(k) clearance under submission number K011147, sponsored by Cavitat Medical Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2002-02-15.
- Submission: K011147
- Applicant / Sponsor: Cavitat Medical Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.1800
- Decision date: 2002-02-15
Classification & Regulation
This clearance is catalogued under FDA product code EHD and 21 CFR 872.1800, within the Dental review panel as a Class II device.