Clearance Summary
DECUBITUS MATTRESS received FDA 510(k) clearance under submission number K760963, sponsored by Arco Medical Products Co.. 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 1976-11-18.
- Submission: K760963
- Applicant / Sponsor: Arco Medical Products Co.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.5150
- Decision date: 1976-11-18
Classification & Regulation
This clearance is catalogued under FDA product code IKY and 21 CFR 880.5150, within the General Hospital review panel as a Class I device.