Clearance Summary
VERTICAL LIFT received FDA 510(k) clearance under submission number K983526, sponsored by Barnes,Richardson & Colburn. 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 1998-12-11.
- Submission: K983526
- Applicant / Sponsor: Barnes,Richardson & Colburn
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.3930
- Decision date: 1998-12-11
Classification & Regulation
This clearance is catalogued under FDA product code ING and 21 CFR 890.3930, within the Physical Medicine review panel as a Class II device.