Clearance Summary
ZENITH HYLO AND VERTI-LIFT CHIROPRACTIC TABLES received FDA 510(k) clearance under submission number K902971, sponsored by Williams Manufacturing Co.. 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 1990-07-26.
- Submission: K902971
- Applicant / Sponsor: Williams Manufacturing Co.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.3760
- Decision date: 1990-07-26
Classification & Regulation
This clearance is catalogued under FDA product code INQ and 21 CFR 890.3760, within the Physical Medicine review panel as a Class I device.