Clearance Summary
STRYKER 1990 LIBERTY ELECTRIC CRITICAL CARE BED received FDA 510(k) clearance under submission number K875037, sponsored by Stryker Corp.. 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 1988-02-11.
- Submission: K875037
- Applicant / Sponsor: Stryker Corp.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5100
- Decision date: 1988-02-11
Classification & Regulation
This clearance is catalogued under FDA product code FNL and 21 CFR 880.5100, within the General Hospital review panel as a Class II device.