Clearance Summary
UROK ROCKING WHEELCHAIR, MODEL 700-4XX received FDA 510(k) clearance under submission number K052548, sponsored by Amg Medical, Inc.. 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 2006-01-06.
- Submission: K052548
- Applicant / Sponsor: Amg Medical, Inc.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.3850
- Decision date: 2006-01-06
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.