Clearance Summary
HUAYI K-SERIES LIGHTWEIGHT WHEELCHAIR K3/K4 received FDA 510(k) clearance under submission number K091482, sponsored by Danyang Huayi Medical Supply & Equipment Co, Ltd.. 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 2009-07-06.
- Submission: K091482
- Applicant / Sponsor: Danyang Huayi Medical Supply & Equipment Co, Ltd.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.3850
- Decision date: 2009-07-06
Classification & Regulation
This clearance is catalogued under FDA product code IOR and 21 CFR 890.3850, within the Physical Medicine review panel as a Class I device.