Clearance Summary
THE VERSA-BED received FDA 510(k) clearance under submission number K792298, sponsored by First & Ten, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1979-12-20.
- Submission: K792298
- Applicant / Sponsor: First & Ten, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.5120
- Decision date: 1979-12-20
Classification & Regulation
This clearance is catalogued under FDA product code FNJ and 21 CFR 880.5120, within the General Hospital review panel as a Class I device.