Clearance Summary
DOUBLE SUPPORT PONCHO/SLIDER PONCHO received FDA 510(k) clearance under submission number K963447, sponsored by Skil-Care 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 1996-10-07.
- Submission: K963447
- Applicant / Sponsor: Skil-Care Corp.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6760
- Decision date: 1996-10-07
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.