DeviceClearance

Product code ING— Physical Medicine

AIR CUSHIONED AUTO WHEELCHAIR LIFT ACL-200/AG-Z2

Classification name
Elevator, Wheelchair, Portable
Device class
Class 2
Regulation
21 CFR 890.3930
Advisory panel
Physical Medicine
Total cleared
29
First cleared
Most recent

FDA classification definition

“A motorized lift device that is not permanently mounted in one location and that is intended for medical purposes to provide a means to move a person with impaired mobility, with or without a wheelchair, from one level to another (e.g., portable platform lifts, attendant-operated stair climbing devices for wheelchairs).”

— U.S. Food and Drug Administration, device classification record for product code ING under 21 CFR 890.3930, via openFDA

Market context for product code ING

FDA has cleared 29 devices under product code ING between 1985 and 2012, filed by 19 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

last 15 years

Top applicants under product code ING

Adverse events under product code ING

product code ING
Death
3
Total
3

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recent clearances under product code ING

Data sourced from openFDA. This site is unofficial and independent of the FDA.