Clearance Summary
KUDO (POWERED ROTATION BED) received FDA 510(k) clearance under submission number K905390, sponsored by Kinetic Concepts, Inc.. 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 1991-01-08.
- Submission: K905390
- Applicant / Sponsor: Kinetic Concepts, Inc.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.5225
- Decision date: 1991-01-08
Classification & Regulation
This clearance is catalogued under FDA product code IKZ and 21 CFR 890.5225, within the Physical Medicine review panel as a Class II device.