Clearance Summary
TORSO/WAIST RESTRAINT received FDA 510(k) clearance under submission number K963374, sponsored by Morrison Medical Products. 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 1996-11-08.
- Submission: K963374
- Applicant / Sponsor: Morrison Medical Products
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6760
- Decision date: 1996-11-08
Classification & Regulation
This clearance is catalogued under FDA product code FMQ and 21 CFR 880.6760, within the General Hospital review panel as a Class I device.