Clearance Summary
RIFTON MOR219 19 & RIFTON MOR225 25 received FDA 510(k) clearance under submission number K921817, sponsored by Rifton Equipment For the Handicapped. 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 1992-04-29.
- Submission: K921817
- Applicant / Sponsor: Rifton Equipment For the Handicapped
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.3100
- Decision date: 1992-04-29
Classification & Regulation
This clearance is catalogued under FDA product code INM and 21 CFR 890.3100, within the Physical Medicine review panel as a Class I device.